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destructive Skelid (Oral) Generic Name: tiludronate (Oral route) tye-loo-DROE-nate Overview Side Effects Dosage Professional Interactions More Pregnancy Warnings Breastfeeding Warnings User Reviews Support Group Q & A Commonly used brand name(s) In the U.S. Skelid Available Dosage Forms: Tablet Therapeutic Class: Calcium Regulator Chemical Class: Bisphosphonate Slideshow A Joint Effort: A Provider's Guide To Orthopedic Pain Options Uses For Skelid Tiludronate is used to treat Paget's disease of the bone. This medicine is a bisphosphonate that helps make the bones stronger. This medicine is available only with your doctor's prescription. Before Using Skelid In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered: Allergies Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully. Pediatric Appropriate studies have not been performed on the relationship of age to the effects of tiludronate in the pediatric population. Safety and efficacy have not been established. Geriatric Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of tiludronate in the elderly. Pregnancy Pregnancy Category Explanation All Trimesters C Animal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women. Breast Feeding There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding. Interactions with Medicines Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine. Interactions with Food/Tobacco/Alcohol Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive. Other Medical Problems The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially: Anemia or Blood clotting problems or Cancer or use of cancer medicines or Dental or tooth problems or Infection or Poor oral hygiene Use with caution. May increase risk for a serious side effect with the jaw. Barrett's esophagus or Bone or joint pain or Esophagus problems (e.g., difficulty with swallowing or inflammation) or Muscle pain, severe or Stomach or bowel problems (e.g., gastritis, heartburn or ulcers) Use with caution. May make these conditions worse. Kidney disease Use with caution. The effects may be increased because of slower removal of the medicine from the body. Proper Use of Skelid Take this medicine only as directed by your doctor . Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered. To do so may increase the chance for unwanted effects. Swallow the tablet whole with a large glass (8 ounces) of plain water. Do not drink mineral water, milk, coffee, juice, or any other liquid when you take the tablet. It is best to take this medicine on an empty stomach, either 2 hours before or 2 hours after eating. Do not lie down for at least 30 minutes after taking this medicine. It is important that you eat a well-balanced diet with an adequate amount of calcium and vitamin D while you are taking this medicine. Your doctor can help you choose the best diet for your condition. If you use calcium supplements, mineral supplements, indomethacin, or aspirin, take them either 2 hours before or 2 hours after you take tiludronate. If you use antacids, wait at least 2 hours after your dose before you take the antacid. If you take these medicines together with tiludronate, it may keep the medicine from working properly. Tiludronate takes up to 3 months to work. If you feel that the medicine is not working, talk to your doctor. Do not stop taking the medicine without checking with your doctor. Dosing The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so. The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine. For oral dosage form (tablets): For treating Paget's disease: Adults 400 milligrams (mg) once a day for at least 3 months. Children Use and dose must be determined by your doctor. Missed Dose If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses. Storage Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing. Ask your healthcare professional how you should dispose of any medicine you do not use. Keep out of the reach of children. Do not keep outdated medicine or medicine no longer needed. Precautions While Using Skelid It is very important that your doctor check your progress at regular visits . This will allow your doctor to see if the medicine is working properly and to decide if you should continue to take it. . This medicine can irritate your esophagus. Stop taking this medicine and call your doctor right away if you have severe heartburn (new or worse than usual), pain with swallowing, chest pain, trouble with swallowing, or feel like food is getting stuck in your esophagus. It is important that you tell all of your doctors or dentist that you are taking tiludronate. Make sure you tell your doctor about any new medical problems, especially with your teeth or jaw. If you have dental procedures while using this medicine, you may have an increased chance for serious jaw problems. Tell your doctor right away if you have any jaw tightness, swelling, numbness, or pain while using this medicine. This medicine can cause muscle or joint pain that in some cases is very severe. Tell your doctor right away if you have bone, joint, or muscle pain while using this medicine. Skelid Side Effects Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention. Check with your doctor immediately if any of the following side effects occur: More common Cough fever head congestion hoarseness or other voice changes nasal congestion runny nose sneezing sore throat Less common Blindness blurred or decreased vision burning, dry, or itching eyes chest pain discharge or excessive tearing eye pain headache redness, pain, or swelling of the eye, eyelid, or inner lining of the eyelid swelling of the face, feet, or lower legs unusual weight gain Rare Bladder pain blistering, peeling, or loosening of the skin bloody or cloudy urine difficult, burning, or painful urination dizziness or lightheadedness fainting feeling of constant movement of self or surroundings frequent urge to urinate headache itching red skin lesions, often with a purple center lower back or side pain nervousness pain or swelling in the arms or legs without any injury pounding in the ears sensation of spinning slow or fast heartbeat sores, ulcers, or white spots in the mouth or on the lips Get emergency help immediately if any of the following symptoms of overdose occur: Symptoms of overdose Abdominal or stomach cramps confusion convulsions difficulty with breathing irregular heartbeats mood or mental changes muscle cramps in the hands, arms, feet, legs, or face numbness and tingling around the mouth, fingertips, or feet shortness of breath tremor Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them: More common Back pain body pain (general) diarrhea nausea upset stomach Less common Bone fractures burning, crawling, itching, numbness, prickling, "pins and needles", or tingling feelings confusion difficulty having a bowel movement (stool) dizziness dry skin hair loss increased thirst increased urination joint pain loss of appetite muscle cramps or spasms muscle pain red or irritated eyes skin rash stomach gas throat pain tooth disorder trouble thinking vomiting Rare Dry mouth fear or nervousness feeling of warmth lack or loss of strength redness of the face, neck, arms and occasionally, upper chest sleepiness or unusual drowsiness stomach pain sleeplessness trouble sleeping unable to sleep unusual tiredness or weakness Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088. Side Effects (complete list) The information contained in the Truven Health Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you. The use of the Truven Health products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Truven Health and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, TRUVEN HEALTH MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Truven Health does not assume any responsibility or risk for your use of the Truven Health products. Copyright 2017 Truven Health Analytics, Inc. All Rights Reserved. Next Side Effects Print this page Add to My Med List More about Skelid (tiludronate) Side Effects During Pregnancy or Breastfeeding Dosage Information Drug Interactions Support Group 0 Reviews Add your own review/rating Drug class: bisphosphonates Professional resources Skelid (FDA) Related treatment guides Paget's Disease} Drug Status Availability Discontinued C Pregnancy Category Risk cannot be ruled out N/A CSA Schedule Not a controlled drug 10 + years Approval History FDA approved 1997 Drug Class Bisphosphonates Related Drugs Paget's Disease alendronate , Fosamax , Actonel , Reclast , Zometa , risedronate , zoledronic acid , calcitonin , Miacalcin , Aredia , pamidronate , Fortical , Binosto , etidronate , Aclasta , Miacalcin Nasal , Didronel , tiludronate , More... Skelid Rating No Reviews - Be the first! No Reviews - Be the first! Not Rated - Be the first! Related Questions & Answers Paget's Disease - I was diagnosed with Pagets Disease some years ago. 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one and all Skin Bleaching-Sunscreen Generic Name: Hydroquinone (HYE droe kwin one) Brand Name: Aclaro PD, Aclaro, Alphaquin HP, AMBI Fade, Blanche, ...show all 25 brand names. EpiQuin Micro, Esoterica Daytime, Esoterica Facial, Esoterica Fade Nighttime, Esoterica Sensitive Skin, Exuviance Lightening Complex, Hydroquinone Time Release, Lustra, Lustra-AF, Lustra-Ultra, Melpaque HP, Melquin 3, Melquin HP, NeoCeuticals Post-Acne Fade, NeoStrata HQ Skin Lightening, Nuquin HP, Remergent HQ, Skin Bleaching, Skin Bleaching-Sunscreen, TL Hydroquinone Overview Side Effects Dosage Professional Pregnancy More User Reviews Support Group Q & A Pricing & Coupons Uses of Skin Bleaching-Sunscreen: It is used to lighten the skin where there are changes in color. Slideshow A Joint Effort: A Provider's Guide To Orthopedic Pain Options What do I need to tell my doctor BEFORE I take Skin Bleaching-Sunscreen? If you have an allergy to hydroquinone or any other part of Skin Bleaching-Sunscreen (hydroquinone). If you are allergic to any drugs like this one, any other drugs, foods, or other substances. Tell your doctor about the allergy and what signs you had, like rash; hives; itching; shortness of breath; wheezing; cough; swelling of face, lips, tongue, or throat; or any other signs. This medicine may interact with other drugs or health problems. Tell your doctor and pharmacist about all of your drugs (prescription or OTC, natural products, vitamins) and health problems. You must check to make sure that it is safe for you to take this medicine with all of your drugs and health problems. Do not start, stop, or change the dose of any drug without checking with your doctor. What are some things I need to know or do while I take Skin Bleaching-Sunscreen? Tell all of your health care providers that you take Skin Bleaching-Sunscreen. This includes your doctors, nurses, pharmacists, and dentists. After stopping this medicine, some of the color change may come back. If you have a sulfite allergy, talk with your doctor. This medicine may cause harm if swallowed. If Skin Bleaching-Sunscreen is swallowed, call a doctor or poison control center right away. Avoid sun, sunlamps, and tanning beds. Use sunscreen and wear clothing and eyewear that protects you from the sun. Tell your doctor if you are pregnant or plan on getting pregnant. You will need to talk about the benefits and risks of using this medicine while you are pregnant. Tell your doctor if you are breast-feeding. You will need to talk about any risks to your baby. How is this medicine (Skin Bleaching-Sunscreen) best taken? Use Skin Bleaching-Sunscreen as ordered by your doctor. Read all information given to you. Follow all instructions closely. Do not take this medicine by mouth. Use on your skin only. Keep out of your mouth, nose, and eyes (may burn). Wash your hands before and after use. Do not wash your hands after use if putting this on your hand. Clean affected part before use. Make sure to dry well. Put a thin layer on the affected skin and rub in gently. Practice good skin care and avoid the sun. Do not use coverings (bandages, dressings, make-up) unless told to do so by the doctor. Do not use on irritated skin. What do I do if I miss a dose? Put on a missed dose as soon as you think about it. If it is close to the time for your next dose, skip the missed dose and go back to your normal time. Do not put on 2 doses or extra doses. Dosage Information (comprehensive) What are some side effects that I need to call my doctor about right away? WARNING/CAUTION: Even though it may be rare, some people may have very bad and sometimes deadly side effects when taking a drug. Tell your doctor or get medical help right away if you have any of the following signs or symptoms that may be related to a very bad side effect: Signs of an allergic reaction, like rash; hives; itching; red, swollen, blistered, or peeling skin with or without fever; wheezing; tightness in the chest or throat; trouble breathing or talking; unusual hoarseness; or swelling of the mouth, face, lips, tongue, or throat. Very bad skin irritation. Change in color of skin to blue-black. Itching. Blisters or sores. What are some other side effects of Skin Bleaching-Sunscreen? All drugs may cause side effects. However, many people have no side effects or only have minor side effects. Call your doctor or get medical help if any of these side effects or any other side effects bother you or do not go away: Dry skin. Skin irritation. Redness. These are not all of the side effects that may occur. If you have questions about side effects, call your doctor. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088. You may also report side effects at http://www.fda.gov/medwatch. Side Effects (complete list) If OVERDOSE is suspected: If you think there has been an overdose, call your poison control center or get medical care right away. Be ready to tell or show what was taken, how much, and when it happened. How do I store and/or throw out Skin Bleaching-Sunscreen? Store at room temperature. Store in a dry place. Do not store in a bathroom. Keep all drugs in a safe place. Keep all drugs out of the reach of children and pets. Check with your pharmacist about how to throw out unused drugs. Consumer Information Use and Disclaimer If your symptoms or health problems do not get better or if they become worse, call your doctor. Do not share your drugs with others and do not take anyone else's drugs. Keep a list of all your drugs (prescription, natural products, vitamins, OTC) with you. Give this list to your doctor. Talk with the doctor before starting any new drug, including prescription or OTC, natural products, or vitamins. Some drugs may have another patient information leaflet. Check with your pharmacist. If you have any questions about Skin Bleaching-Sunscreen, please talk with your doctor, nurse, pharmacist, or other health care provider. If you think there has been an overdose, call your poison control center or get medical care right away. Be ready to tell or show what was taken, how much, and when it happened. This information should not be used to decide whether or not to take this medicine or any other medicine. Only the healthcare provider has the knowledge and training to decide which medicines are right for a specific patient. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about Skin Bleaching-Sunscreen. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to this medicine. This information is not specific medical advice and does not replace information you receive from the healthcare provider. You must talk with the healthcare provider for complete information about the risks and benefits of using Skin Bleaching-Sunscreen. Review Date: November 1, 2017 Next Side Effects Print this page Add to My Med List More about hydroquinone topical Side Effects During Pregnancy Dosage Information Support Group Pricing & Coupons 5 Reviews Add your own review/rating Drug class: topical depigmenting agents Consumer resources Hydroquinone topical Hydroquinone Hydroquinone with Sunscreen Cream and Gel Other brands: Hydroquinone and Sunscreen , Lustra , Melquin HP , Melpaque HP , ... +23 more Professional resources Hydroquinone (AHFS Monograph) ... +4 more Related treatment guides Dermatological Disorders Drug Status Rx OTC Availability Rx and/or OTC C Pregnancy Category Risk cannot be ruled out N/A CSA Schedule Not a controlled drug Hydroquinone topical Rating 5 User Reviews 2.8 /10 5 User Reviews 2.8 Rate it! Manufacturers Perrigo Company Acella Pharmaceuticals, LLC Drug Class Topical depigmenting agents Related Drugs Dermatological Disorders triamcinolone , clobetasol topical , betamethasone , Temovate , Diprolene , Analpram-HC , Celestone , urea topical , Clobex , Valisone , Proctofoam HC , sodium hyaluronate topical , hydroquinone topical , Olux , Betamethacot , Diprosone , salicylic acid topical , Melamin , Diprolene AF , Celestone Soluspan , Analpram E , Clobevate , More... obligations


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leading [30:<30 mL/min (see CLINICAL PHARMACOLOGY, Renal Insufficiency ). Osteonecrosis, primarily in the jaw, has been reported in patients treated with bisphosphonates. Most cases have been in cancer patients undergoing dental procedures, but some have occurred in patients with postmenopausal osteoporosis or other diagnoses. Known risk factors for osteonecrosis include a diagnosis of cancer, concomitant therapies (e.g., chemotherapy, radiotherapy, corticosteroids), and co-morbid disorders (e.g., anemia, coagulopathy, infection, pre-existing dental disease). Most reported cases have been in patients treated with bisphosphonates intravenously but some have been in patients treated orally. For patients who develop osteonecrosis of the jaw (ONJ) while on bisphosphonate therapy, dental surgery may exacerbate the condition. For patients requiring dental procedures, there are no data available to suggest whether discontinuation of bisphosphonate treatment reduces the risk of ONJ. Clinical judgement of the treating physician should guide the management plan of each patient based on individual benefit/risk assessment. Musculoskeletal Pain In post marketing experience, severe and occasionally incapaciting bone, joint, and/or muscle pain has been reported in patients taking bisphosphonates. However, such reports have been infrequent. This category of drugs includes Skelid. The time to onset of symptoms varied from one day to several months after starting the drug. Most patients had relief of symptoms after stopping. A subset had recurrence of symptoms when rechallenged with the same drug or another bisphosphonate. Information for Patients Patients receiving Skelid should be instructed to: Take Skelid with 6 to 8 ounces of plain water. Not lie down for at least 30 minutes after taking this medication. Skelid should not be taken within 2 hours of food. Maintain adequate vitamin D and calcium intake. Calcium supplements, aspirin, and indomethacin should not be taken within 2 hours before or 2 hours after Skelid. Aluminum- or magnesium-containing antacids, if needed, should be taken at least 2 hours after taking Skelid. Drug Interactions The bioavailability of Skelid is decreased 80% by calcium, when calcium and Skelid are administered at the same time, and 60% by some aluminum- or magnesium-containing antacids, when administered 1 hour before Skelid. Aspirin may decrease bioavailability of Skelid by up to 50% when taken 2 hours after Skelid. The bioavailability of Skelid is increased 2 4 fold by indomethacin but is not significantly altered by coadministration of diclofenac. The pharmacokinetic parameters of digoxin are not significantly modified by Skelid coadministration. In vitro studies show that tiludronate does not displace warfarin from its binding site on protein. Carcinogenesis, Mutagenesis, Impairment of Fertility Carcinogenicity studies have not yet been completed. Tiludronate was not genotoxic in the following assays: an in vitro microbial mutagenesis assay with and without metabolic activation, a human lymphocyte assay, a yeast cell assay for forward mutation and mitotic crossing over, or the in vivo mouse micronucleus test. Tiludronate had no effect on rat fertility (male or female) at exposures up to two times the 400 mg/day human dose, based on surface area, mg/m 2 (75 mg/kg/day tiludronic acid dose). Pregnancy Pregnancy Category C In a teratology study in rabbits dosed during days 6 18 of gestation at 42 mg/kg/day and 130 mg/kg/day (2 and 5 times the 400 mg/day human dose based on body surface area), there was dose-related scoliosis likely attributable to the pharmacologic properties of the drug. Mice receiving 375 mg/kg/day tiludronic acid (7 times the 400 mg/day human dose based on body surface area, mg/m 2 ) for days 6 15 of gestation showed slight maternal toxicity (decreased body weight gain), increased post-implantation loss, decreased number of fetuses/dam, and decreased fetus body weight. Uncommon malformations of the paw (shortened or missing digits, blood blisters between or in place of digits) were present in six fetuses at 375 mg/kg/day, all from the same litter. Maternal toxicity (decreased body weight) was also observed in a teratology study in rats dosed during days 6 18 of gestation at 375 mg/kg/day tiludronic acid (10 times the 400 mg/day human dose based on body surface area, mg/m 2 ). There were reduced percent implantations, increased postimplantation loss, and increased intra-uterine deaths in the rats. There were no teratogenic effects on fetuses. Protracted parturition and maternal death, presumably due to hypocalcemia, occurred at 75 mg/kg/day tiludronic acid (two times the 400 mg/day human dose based on body surface area, mg/m 2 ) when rats were treated from day 15 of gestation to day 25 postpartum. There are no adequate and well-controlled studies in pregnant women. Skelid should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Bisphosphonates are incorporated into the bone matrix, from where they are gradually released over periods of weeks to years. The extent of bisphosphonate incorporation into adult bone, and hence, the amount available for release back into the systemic circulation, is directly related to the total dose and duration of bisphosphonate use. Although there are no data on fetal risk in humans, bisphosphonates do cause fetal harm in animals, and animal data suggest that uptake of bisphosphonates into fetal bone is greater than into maternal bone. Therefore, there is a theoretical risk of fetal harm (e.g., skeletal and other abnormalities) if a woman becomes pregnant after completing a course of bisphosphonate therapy. The impact of variables such as time between cessation of bisphosphonate therapy to conception, the particular bisphosphonate used, and the route of administration (intravenous versus oral) on this risk has not been established. Nursing Mothers It is not known whether tiludronate is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Skelid is administered to a nursing woman. Pediatric Use Safety and effectiveness of Skelid in pediatric patients have not been established. Adverse Reactions The safety of Skelid has been studied in more than 1100 patients, and the adverse experience profile is similar between controlled and uncontrolled clinical trials. Adverse events occurring in placebo-controlled trials of pagetic patients treated with Skelid 400 mg/day are presented in the table below. The most frequently occurring adverse events in patients who received Skelid 400 mg/day were in the gastrointestinal body system: nausea (9.3%), diarrhea (9.3%), and dyspepsia (5.3%). Adverse events associated with Skelid usually have been mild, and generally have not required discontinuation of therapy. In two placebo-controlled trials, 1.3% of patients receiving 400 mg Skelid and 5.4% of patients receiving placebo discontinued therapy due to any clinical adverse event. Adverse Events * (%) Reported in> 2% of Pagetic Patients from Placebo-Controlled Studies Skelid 400 mg/day (n=75) Placebo (n=74) * Reported using WHO terminology All events reported, irrespective of causality BODY AS A WHOLE Pain 21.3 23.0 Back Pain 8.0 8.1 Accidental Injury 4.0 2.7 Influenza-like Symptoms 4.0 5.4 Chest Pain 2.7 0 Peripheral Edema 2.7 1.4 CARDIOVASCULAR, GENERAL Dependent Edema 2.7 0 Central and Peripheral Nervous Systems Headache 6.7 12.2 Dizziness 4.0 6.8 Paresthesia 4.0 0 ENDOCRINE Hyperparathyroidism 2.7 0 GASTROINTESTINAL Diarrhea 9.3 4.1 Nausea 9.3 5.4 Dyspepsia 5.3 8.1 Vomiting 4.0 0 Flatulence 2.7 0 Tooth Disorder 2.7 1.4 Metabolic and Nutritional Vitamin D Deficiency 2.7 2.7 Musculoskeletal System Arthralgia 2.7 5.4 Arthrosis 2.7 0 Resistance Mechanism Infection 2.7 0 Respiratory System Rhinitis 5.3 0 Sinusitis 5.3 1.4 Upper Respiratory Tract Infection 5.3 14.9 Coughing 2.7 2.7 Pharyngitis 2.7 1.4 Skin and Appendage Rash 2.7 1.4 Skin Disorder 2.7 1.4 Vision Cataract 2.7 0 Conjunctivitis 2.7 0 Glaucoma 2.7 0 Other adverse events not listed in the table above but reported in 1% of pagetic patients treated with Skelid in all clinical trials of at least one month duration, regardless of dose and causality assessment, are listed below. The adverse event terms within each body system are listed in the order of decreasing frequency occurring in the population. Body as a Whole: Asthenia, syncope, fatigue Cardiovascular: Hypertension Central and Peripheral Nervous Systems: Vertigo, involuntary muscle contractions Gastrointestinal: Abdominal pain, constipation, dry mouth, gastritis Musculoskeletal: Fracture pathological Psychiatric: Anorexia, somnolence, anxiety, nervousness, insomnia Respiratory System: Bronchitis Skin and Appendages: Pruritus, increased sweating Urinary System: Urinary tract infection Vascular (extracardiac): Flushing Stevens-Johnson type syndrome has been observed rarely; the causality relationship of this to Skelid has not been established. Overdosage Based on the known action of tiludronate, hypocalcemia is a potential consequence of Skelid overdose. In one patient with hypercalcemia of malignancy, intravenous administration of high doses of Skelid (800 mg/day total dose, 6 mg/kg/day for 2 days) was associated with acute renal failure and death. No specific information is available on the treatment of overdose with Skelid. Dialysis would not be beneficial. Standard medical practices may be used to manage renal insufficiency or hypocalcemia, if signs of these develop. Skelid Dosage and Administration A single 400-mg daily oral dose of Skelid, taken with 6 to 8 ounces of plain water only, should be administered for a period of 3 months. Beverages other than plain water (including mineral water), food (see below), and some medications (see PRECAUTIONS, Drug Interactions ) are likely to reduce the absorption of Skelid (see CLINICAL PHARMACOLOGY, Pharmacokinetics ). Patients should not lie down for at least 30 minutes after taking this medication. In patients who cannot comply with dosing instructions due to mental or physical disability, therapy with Skelid should be used under appropriate supervision (See WARNINGS ). Skelid should not be taken within 2 hours of food. Calcium or mineral supplements should be taken at least 2 hours before or two hours after Skelid. Aluminum- or magnesium-containing antacids, if needed, should be taken at least two hours after taking Skelid. Skelid should not be taken within 2 hours of indomethacin. Following therapy, allow an interval of 3 months to assess response. Specific data regarding retreatment are limited, although results from uncontrolled studies indicate favorable biochemical improvement similar to initial Skelid treatment. How is Skelid Supplied Skelid is supplied as white to practically white, biconvex round tablets containing 240 mg tiludronate disodium, which is the molar equivalent of 200 mg tiludronic acid. Skelid tablets are engraved with "S.W" on one side and "200" on the other side and packaged in foil strips in cartons of 56 tablets per carton (0024-1800-16). Storage Skelid should be stored at 25 C (77 F); excursions permitted to 15 C to 30 C (59 F to 86 F) [see USP Controlled Room Temperature]. Tablets should not be removed from the foil strips until they are to be used. sanofi-aventis U.S. LLC Bridgewater, NJ 08807 Country of origin: France Revised March 2010 2010 sanofi-aventis U.S. LLC PRINCIPAL DISPLAY PANEL - 200 mg Tablet Carton S-165 NDC 0024-1800-16 56 Tablets Skelid tiludronate disodium 200 mg Each tablet contains 240 mg tiludronate disodium, equivalent to 200 mg tiludronic acid. Rx only sanofi aventis Skelid tiludronate disodium tablet Product Information Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0024-1800 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength tiludronate disodium (tiludronic acid) tiludronic acid 200 mg Inactive Ingredients Ingredient Name Strength sodium lauryl sulfate crospovidone magnesium stearate lactose monohydrate Product Characteristics Color WHITE Score no score Shape ROUND Size 9mm Flavor Imprint Code S;W;200 Contains Packaging # Item Code Package Description 1 NDC:0024-1800-16 56 TABLET (TABLET) in 1 CARTON Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020707 03/07/1997 Labeler - sanofi-aventis U.S. LLC (824676584) Establishment Name Address ID/FEI Operations Sanofi Winthrop Industrie 763683216 MANUFACTURE Revised: 03/2012 sanofi-aventis U.S. LLC Next Interactions Print this page Add to My Med List More about Skelid (tiludronate) Side Effects During Pregnancy or Breastfeeding Dosage Information Drug Interactions Support Group 0 Reviews Add your own review/rating Drug class: bisphosphonates Consumer resources Skelid (Advanced Reading) Related treatment guides Paget's Disease ]} FEATURED: CAR-T Cell Therapy Overview Mechanism of Action KTE-C19 Studies KTE-C19 Cancer Targets Adverse Events Manufacturing Drug Status Availability Discontinued C Pregnancy Category Risk cannot be ruled out N/A CSA Schedule Not a controlled drug 10 + years Approval History FDA approved 1997 Drug Class Bisphosphonates Related Drugs bisphosphonates alendronate , Fosamax , Boniva , Actonel , Reclast , ibandronate Paget's Disease alendronate , Fosamax , Actonel , Reclast , Zometa , risedronate , zoledronic acid , calcitonin , Miacalcin , Aredia , pamidronate , Fortical , Binosto , etidronate , Aclasta , Miacalcin Nasal , Didronel , tiludronate , More... 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pharmaceuticals Skeeter Stik Generic Name: benzocaine topical (BENZ oh kane TOP ik al) Brand Name: Americaine, Anacaine, Anbesol Gel, Benzodent, Cepacol Ultra, Dent-O-Kain, Dermoplast, Hurricaine, Kank-a, Lanacane, Medicone Maximum Strength, Numzident, Num-Zit, Orabase, Orajel, Oral Pain Relief, Outgro Pain Relief, Retre-Gel, Skeeter Stik, Solarcaine Aerosol, Sting-Kill, Topex, zilactin-B Overview Side Effects Dosage Interactions Pregnancy More Breastfeeding Warnings User Reviews Support Group Q & A What is Skeeter Stik (benzocaine topical)? Benzocaine is a local anesthetic (numbing medication). It works by blocking nerve signals in your body. Benzocaine topical is used to reduce pain or discomfort caused by minor skin irritations, sore throat, sunburn, teething pain, vaginal or rectal irritation, ingrown toenails, hemorrhoids, and many other sources of minor pain on a surface of the body. Benzocaine is also used to numb the skin or surfaces inside the mouth, nose, throat, vagina, or rectum to lessen the pain of inserting a medical instrument such as a tube or speculum. There are many brands and forms of benzocaine topical available and not all brands are listed on this leaflet. Benzocaine topical may also be used for purposes not listed in this medication guide. Slideshow ADHD and Your Child: Signs and Treatment Options What is the most important information I should know about Skeeter Stik (benzocaine topical)? Benzocaine topical used in the mouth or throat may cause methemoglobinemia (met-HEEM-oh glo-bin-EE-mee-a), a life-threatening condition in which the amount of oxygen in your blood stream becomes dangerously low. Do not use benzocaine topical if you have ever had methemoglobinemia. GET EMERGENCY MEDICAL HELP IF YOU HAVE SYMPTOMS OF METHEMOGLOBINEMIA : headache, tired feeling, confusion, fast heart rate, and feeling light-headed or short of breath, with a pale, blue, or gray appearance of your skin, lips, or fingernails. Do not use this medicine on a child younger than 2 years old without medical advice. An overdose of numbing medications can cause fatal side effects if too much of the medicine is absorbed through your skin and into your blood. Use the smallest amount of this medication needed. What should I discuss with my healthcare provider before using Skeeter Stik (benzocaine topical)? Do not use benzocaine topical if you have ever had methemoglobinemia in the past. An overdose of numbing medications can cause fatal side effects if too much of the medicine is absorbed through your skin and into your blood. This is more likely to occur when using a numbing medicine without the advice of a medical doctor (such as during a cosmetic procedure like laser hair removal). Be aware that many cosmetic procedures are performed without a medical doctor present. Ask a doctor or pharmacist if it is safe for you to use this medicine if you have: asthma, bronchitis, emphysema, or other breathing disorder; heart disease; a personal or family history of methemoglobinemia, or any genetic (inherited) enzyme deficiency; or if you smoke. It is not known whether benzocaine topical will harm an unborn baby. Ask a doctor before using this medicine if you are pregnant. It is not known whether benzocaine topical passes into breast milk or if it could affect a nursing baby. Ask a doctor before using this medicine if you are breast-feeding. Do not use this medicine on a child younger than 2 years old without medical advice. How should I use Skeeter Stik (benzocaine topical)? Use exactly as directed on the label, or as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended. Use the smallest amount of medicine needed to numb the skin or relieve pain. Do not use large amounts of benzocaine topical, or cover treated skin areas with a bandage or plastic wrap without medical advice. Your body may absorb more of this medicine if you use too much, if you apply it over large skin areas, or if you apply heat, bandages, or plastic wrap to treated skin areas. Skin that is cut or irritated may also absorb more topical medication than healthy skin. Do not use benzocaine topical to treat large skin areas or deep puncture wounds. Avoid using the medicine on skin that is raw or blistered, such as a severe burn or abrasion. Read all patient information, medication guides, and instruction sheets provided to you. Ask your doctor or pharmacist if you have any questions. To treat minor skin conditions, apply a thin layer of benzocaine topical to the affected area. If using the spray, hold the container 6 to 12 inches away from the skin. Do not spray this medication onto your face. Spray it instead on your hands and then rub it onto the face, avoiding contact with your eyes. To treat hemorrhoids, apply the medication up to 6 times per day. Clean the area with soap and water before applying benzocaine topical. Wash your hands before and after inserting a rectal suppository. Do not take a rectal suppository by mouth. It is for use only in your rectum. Try to empty your bowel and bladder just before using the benzocaine suppository. Remove the wrapper before inserting the suppository. Avoid handling the suppository too long or it will melt in your hands. Lie on your back with your knees up toward your chest. Gently insert the suppository into your rectum about 1 inch, pointed tip first. For best results, stay lying down for a few minutes. The suppository will melt quickly and you should feel little or no discomfort while holding it in. Avoid using the bathroom for at least an hour after using the suppository. Call your doctor if your symptoms do not improve or if they get worse within the first 7 days of using benzocaine topical. Also call your doctor if your symptoms had cleared up but then came back. If you are treating a sore throat, call your doctor if the pain is severe or lasts longer than 2 days, especially if you also develop a fever, headache, skin rash, swelling, nausea, vomiting, cough, or breathing problems. Store at room temperature away from moisture and heat. Do not freeze. What happens if I miss a dose? Since benzocaine topical is used when needed, you may not be on a dosing schedule. If you are on a schedule, use the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not use extra medicine to make up the missed dose. What happens if I overdose? Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose of benzocaine topical applied to the skin can cause life-threatening side effects such as uneven heartbeats, seizure (convulsions), coma, slowed breathing, or respiratory failure (breathing stops). What should I avoid while using Skeeter Stik (benzocaine topical)? Avoid eating within 1 hour after using benzocaine topical on your gums or inside your mouth. Benzocaine topical is for use only on the surface of your body, or just inside the mouth, vagina, or rectum. Avoid getting this medication in your eyes. Avoid swallowing the gel, liquid, or ointment while applying it to your gums or the inside of your mouth. The throat spray or oral lozenge may be swallowed gradually during use. Skeeter Stik (benzocaine topical) side effects Benzocaine topical used in the mouth or throat may cause a rare but life-threatening condition called methemoglobinemia. In this condition, the amount of oxygen in your blood stream becomes dangerously low . This condition may occur after only one use of benzocaine or after several uses. Signs and symptoms may occur within minutes or up to 2 hours after using benzocaine topical in the mouth or throat. GET EMERGENCY MEDICAL HELP IF YOU HAVE: headache, tired feeling, confusion; fast heart rate; feeling light-headed or short of breath; and pale, blue, or gray appearance of your skin, lips, or fingernails. Get emergency medical help if you have signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat. Stop using benzocaine topical and call your doctor at once if you have: severe burning, stinging, or sensitivity where the medicine is applied; swelling, warmth, or redness; or oozing, blistering, or any signs of infection. Common side effects may include: mild stinging, burning, or itching where the medicine is applied; skin tenderness or redness; or dry white flakes where the medicine was applied. This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. Side Effects (complete list) What other drugs will affect Skeeter Stik (benzocaine topical)? It is not likely that other drugs you take orally or inject will have an effect on topically applied benzocaine. But many drugs can interact with each other. Tell each of your health care providers about all medicines you use, including prescription and over-the-counter medicines, vitamins, and herbal products. Next Side Effects Print this page Add to My Med List More about Skeeter Stik (benzocaine topical) Side Effects During Pregnancy or Breastfeeding Dosage Information Drug Interactions Support Group En Espaรฑol 1 Review Add your own review/rating Drug class: topical anesthetics Consumer resources Other brands: Orajel , Orabase , Anbesol , Hurricaine , ... +27 more Professional resources Benzocaine topical (AHFS Monograph) Benzocaine Gel (FDA) Related treatment guides Insect Bites Pruritus Where can I get more information? Your pharmacist can provide more information about benzocaine topical. Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed. Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist. Copyright 1996-2012 Cerner Multum, Inc. Version: 6.02. Date modified: December 03, 2017 Last reviewed: March 29, 2017} Drug Status Rx OTC Availability Rx and/or OTC C Pregnancy Category Risk cannot be ruled out N/A CSA Schedule Not a controlled drug Drug Class Topical anesthetics Related Drugs Pruritus hydroxyzine , lidocaine topical , hydrocortisone topical , diphenhydramine , Benadryl , doxepin topical , Vistaril , Atarax , cyproheptadine , Anusol-HC , Proctosol-HC , More... Insect Bites benzocaine topical , Lanacane , Dermoplast , Caladryl Clear , Chiggerex , Sting Relief , More... Skeeter Stik Rating 1 User Review 10 /10 1 User Review 10 Rate it! Help and Support Looking for answers? Ask a question or go join the Skeeter Stik support group to connect with others who have similar interests.} } respectable


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a fireplace Babee Cof Syrup (Oral) for enhancing

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every person Babee Cof Syrup (Oral) Generic Name: dextromethorphan (Oral route) dex-troe-meth-OR-fan Overview Side Effects Dosage Interactions Pregnancy More Breastfeeding Warnings User Reviews Support Group Q & A Commonly used brand name(s) In the U.S. Babee Cof Syrup Benylin Pediatric Formula Children's Pedia Care Creomulsion Creo-Terpin Delsym Dexalone ElixSure Cough Children's Father John's Medicine Miltuss Nycoff Pediacare Pediacare Long-Acting Cough Robafen Cough Robitussin Silphen DM Simply Cough St. Joseph Vicks 44 Cough Relief Available Dosage Forms: Suspension, Extended Release Solution Capsule Syrup Lozenge/Troche Elixir Tablet Liquid Capsule, Liquid Filled Suspension Therapeutic Class: Antitussive Slideshow OTC Medication Use In Pregnancy: Wise or Worrisome? Uses For Babee Cof Syrup Dextromethorphan is used to relieve coughs due to colds or influenza (flu). It should not be used for chronic cough that occurs with smoking, asthma, or emphysema or when there is an unusually large amount of mucus or phlegm (flem) with the cough. Dextromethorphan relieves cough by acting directly on the cough center in the brain. This medicine is available without a prescription. Do not give any over-the-counter (OTC) cough and cold medicine to a baby or child under 4 years of age. Using these medicines in very young children might cause serious or possibly life-threatening side effects . Before Using Babee Cof Syrup In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered: Allergies Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully. Pediatric Although there is no specific information comparing use of dextromethorphan in children with use in other age groups, this medicine is not expected to cause different side effects or problems in children 4 years of age and older than it does in adults. Do not give any over-the-counter (OTC) cough and cold medicine to a baby or child under 4 years of age. Using these medicines in very young children might cause serious or possibly life-threatening side effects . Geriatric Many medicines have not been studied specifically in older people. Therefore, it may not be known whether they work exactly the same way they do in younger adults or if they cause different side effects or problems in older people. There is no specific information comparing use of dextromethorphan in the elderly with use in other age groups. Breast Feeding Studies in women suggest that this medication poses minimal risk to the infant when used during breastfeeding. Interactions with Medicines Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive. Using this medicine with any of the following medicines is not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take. Clorgyline Iproniazid Isocarboxazid Moclobemide Nialamide Pargyline Phenelzine Procarbazine Rasagiline Safinamide Selegiline Toloxatone Tranylcypromine Using this medicine with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines. Alfentanil Almotriptan Amitriptyline Amoxapine Amphetamine Benzphetamine Buprenorphine Bupropion Butorphanol Citalopram Clomipramine Codeine Darunavir Desipramine Desvenlafaxine Dextroamphetamine Dihydrocodeine Dolasetron Doxepin Duloxetine Escitalopram Fentanyl Fluoxetine Fluvoxamine Granisetron Hydrocodone Hydromorphone Hydroxytryptophan Imipramine Levomilnacipran Levorphanol Linezolid Lisdexamfetamine Lorcaserin Memantine Meperidine Methadone Methamphetamine Methylene Blue Milnacipran Mirtazapine Morphine Morphine Sulfate Liposome Nalbuphine Nortriptyline Oxycodone Oxymorphone Palonosetron Panobinostat Paroxetine Pentazocine Protriptyline Remifentanil Sertraline Sibutramine Sufentanil Tapentadol Tramadol Trazodone Trimipramine Venlafaxine Vilazodone Vortioxetine Ziprasidone Using this medicine with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines. Abiraterone Clobazam Haloperidol Quinidine Interactions with Food/Tobacco/Alcohol Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive. Other Medical Problems The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially: Asthma Since dextromethorphan decreases coughing, it makes it difficult to get rid of the mucus that collects in the lungs and airways during asthma Diabetes (sugar diabetes) Some products contain sugar and may affect control of blood glucose monitoring Liver disease Dextromethorphan may build up in the body and cause unwanted effects Chronic bronchitis or Emphysema or Mucus or phlegm with cough Since dextromethorphan decreases coughing, it makes it difficult to get rid of the mucus that may collect in the lungs and airways with some diseases Slowed breathing Dextromethorphan may slow the rate of breathing even further Proper Use of dextromethorphan This section provides information on the proper use of a number of products that contain dextromethorphan. It may not be specific to Babee Cof Syrup. Please read with care. Make certain your health care professional knows if you are on a low-sodium, low-sugar, or any other special diet. Most medicines contain more than their active ingredient, and many liquid medicines contain alcohol. Use this medicine only as directed by your doctor or the directions on the label. Do not use more of it, do not use it more often, and do not use it for a longer time than your doctor or the label says. Although this effect has happened only rarely, dextromethorphan has become habit-forming (causing mental or physical dependence) in some persons who used too much for a long time. Dosing The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so. The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine. For lozenge dosage form: For cough: Adults and children 12 years of age and older 5 to 15 mg every two to four hours, as needed. Children 6 to 12 years of age 5 to 15 mg every two to six hours, as needed. Children 4 to 6 years of age 5 mg every four hours, as needed. Children and infants up to 4 years of age Use is not recommended . For syrup dosage form: For cough: Adults and children 12 years of age and older 30 mg every six to eight hours, as needed. Children 6 to 12 years of age 7 mg every four hours or 15 mg every six to eight hours, as needed. Children 4 to 6 years of age 3.5 mg every four hours or 7.5 mg every six to eight hours, as needed. Children and infants up to 4 years of age Use is not recommended . For extended-release oral suspension dosage form : For cough: Adults and children 12 years of age and older 60 mg every twelve hours, as needed. Children 6 to 12 years of age 30 mg every twelve hours, as needed. Children 4 to 6 years of age 15 mg every twelve hours, as needed. Children and infants up to 4 years of age Use is not recommended . Missed Dose If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses. Storage Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing. Keep out of the reach of children. Do not keep outdated medicine or medicine no longer needed. Precautions While Using Babee Cof Syrup If your cough has not improved after 7 days, if sore throat has not improved after 2 days, if you have a high fever, skin rash, or continuing headache with the cough, or if asthma or high blood pressure is present, check with your doctor. These signs may mean that you have other medical problems. Dissolve lozenges in the mouth with caution, to lessen the risk of choking. Babee Cof Syrup Side Effects Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention. Check with your doctor as soon as possible if any of the following side effects occur: Symptoms of overdose Blurred vision confusion difficulty in urination drowsiness or dizziness nausea or vomiting (severe) shakiness and unsteady walk slowed breathing unusual excitement, nervousness, restlessness, or irritability (severe) Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them: Less common or rare Confusion constipation dizziness (mild) drowsiness (mild) headache nausea or vomiting stomach pain Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088. Side Effects (complete list) The information contained in the Truven Health Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you. The use of the Truven Health products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Truven Health and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, TRUVEN HEALTH MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Truven Health does not assume any responsibility or risk for your use of the Truven Health products. Copyright 2017 Truven Health Analytics, Inc. All Rights Reserved. Next Side Effects Print this page Add to My Med List More about Babee Cof (dextromethorphan) Side Effects During Pregnancy or Breastfeeding Dosage Information Drug Interactions Support Group En Espaรฑol 0 Reviews Add your own review/rating Drug class: antitussives Consumer resources Babee Cof Other brands: Delsym , DexAlone , St. Joseph Cough Suppressant , Vicks Dayquil Cough , ... +13 more Professional resources Dextromethorphan Hydrobromide (AHFS Monograph) Related treatment guides Cough} Drug Status Rx OTC Availability Rx and/or OTC C Pregnancy Category Risk cannot be ruled out N/A CSA Schedule Not a controlled drug Drug Class Antitussives Related Drugs Cough benzonatate , acetaminophen / hydrocodone , diphenhydramine , Benadryl , Mucinex , guaifenesin , Dilaudid , Promethazine DM , hydromorphone , Lortab , codeine , Tessalon Perles , Tessalon , Cheratussin AC , dextromethorphan , Tylenol with Codeine #3 , Mucinex DM , acetaminophen / codeine , codeine / guaifenesin , Tylenol with Codeine , Tussionex Pennkinetic , Hydromet , More... Babee Cof Rating No Reviews - Be the first! No Reviews - Be the first! Not Rated - Be the first! Help and Support Looking for answers? Ask a question or go join the Babee Cof support group to connect with others who have similar interests.} } of what's


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lower your expenses B3-500-Gr Generic Name: niacin (nicotinic acid) (NYE a sin (NIK oh TIN ik AS id)) Brand Name: B-3-50, B3-500-Gr, Niacin SR, Niacor, Niaspan ER, Slo-Niacin Overview Side Effects Dosage Interactions Pregnancy More User Reviews Support Group Q & A What is B3-500-Gr (niacin)? Niacin, also called nicotinic acid, is a B vitamin (vitamin B3). It occurs naturally in plants and animals, and is also added to many foods as a vitamin supplement. Niacin is also present in many multiple vitamins and nutritional supplements. Niacin is used to treat and prevent a lack of natural niacin in the body, and to lower cholesterol and triglycerides (types of fat) in the blood. It is also used to lower the risk of heart attack in people with high cholesterol who have already had a heart attack. Niacin is sometimes used to treat coronary artery disease (also called atherosclerosis). Niacin may also be used for purposes not listed in this medication guide. Slideshow Love Your Dad? Here's 10 Heart-Healthy Gifts For Father's Day What is the most important information I should know about B3-500-Gr (niacin)? You should not take this medication if you are allergic to niacin, or if you have severe liver disease, a stomach ulcer, or active bleeding. Niacin can cause certain side effects, such as flushing (warmth, itching, redness, or tingly feeling under your skin). These effects can be made worse if you drink alcohol or hot beverages shortly after you take niacin. These effects should disappear over time as you keep taking the medication. Avoid getting up too fast from a sitting or lying position, or you may feel dizzy. Get up slowly and steady yourself to prevent a fall. Avoid taking colestipol (Colestid) or cholestyramine (Locholest, Prevalite, Questran) at the same time you take niacin. If you take either of these other medications, take them at least 4 to 6 hours before or after you take niacin. Niacin is only part of a complete program of treatment that may also include diet, exercise, weight control, and other medications. Follow your diet, medication, and exercise routines very closely. What should I discuss with my healthcare provider before taking B3-500-Gr (niacin)? You should not take this medication if you are allergic to niacin, or if you have severe liver disease, a stomach ulcer, or active bleeding. To make sure you can safely take niacin, tell your doctor if you have any of these other conditions: liver or kidney disease; heart disease or uncontrolled angina (chest pain); a stomach ulcer; diabetes; gout; or a muscle disorder such as myasthenia gravis. FDA pregnancy category C. Niacin may be harmful to an unborn baby when the medication is taken at doses to treat high cholesterol or other conditions. Tell your doctor if you are pregnant or plan to become pregnant during treatment. Niacin can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. How should I take B3-500-Gr (niacin)? Use exactly as directed on the label, or as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended. Niacin is sometimes taken at bedtime with a low-fat snack. Follow your doctor's instructions. Niacin can cause certain side effects, such as flushing (warmth, itching, redness, or tingly feeling under your skin). These effects can be made worse if you drink alcohol or hot beverages shortly after you take niacin. These effects should disappear over time as you keep taking the medication. Take niacin with a full glass of cold or cool water. Taking the medication with a hot drink may increase your risk of side effects such as flushing. Do not crush, chew, break, or open an extended-release tablet or capsule. Swallow it whole. Breaking or opening the pill may cause too much of the drug to be released at one time. Niacin extended-release tablets and capsules contain higher strengths of the medicine than the regular niacin tablets. Take only the dose that is correct for the type of niacin tablet or capsule you are using. Niacin can cause you to have unusual results with certain medical tests (urine tests). Tell any doctor who treats you that you are using niacin. If you stop taking niacin for any length of time, talk with your doctor before starting the medication again. You may need to restart the medication at a lower dose. While using niacin, you may need blood tests at your doctor's office. Your kidney or liver function may also need to be checked. Visit your doctor regularly. Niacin is only part of a complete program of treatment that may also include diet, exercise, weight control, and other medications. Follow your diet, medication, and exercise routines very closely. Store at room temperature away from moisture and heat. What happens if I miss a dose? Take the missed dose as soon as you remember. Be sure to take the missed dose with food if you normally take your niacin dose with a meal or snack. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose. What happens if I overdose? Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. Overdose symptoms may include nausea, dizziness, itching, vomiting, upset stomach, and flushing (warmth, redness, or tingly feeling). What should I avoid while taking B3-500-Gr (niacin)? Avoid drinking hot beverages shortly after taking niacin. Hot drinks can worsen niacin's flushing effect (warmth, itching, redness, or tingly feeling under your skin). Avoid drinking alcohol while taking niacin. Alcohol may increase your risk of liver damage, and can also worsen the flushing effects of niacin. Avoid taking colestipol (Colestid) or cholestyramine (Locholest, Prevalite, Questran) at the same time you take niacin. If you take either of these other medications, take them at least 4 to 6 hours before or after you take niacin. Avoid getting up too fast from a sitting or lying position, or you may feel dizzy. Get up slowly and steady yourself to prevent a fall. B3-500-Gr (niacin) side effects Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have any of these serious side effects: feeling like you might pass out; fast, pounding, or uneven heart beats; feeling short of breath; swelling; jaundice (yellowing of your skin or eyes); or muscle pain, tenderness, or weakness with fever or flu symptoms and dark colored urine. If you are diabetic, tell your doctor about any changes in your blood sugar levels. Less serious side effects of niacin include: mild dizziness; warmth, redness, or tingly feeling under your skin; itching, dry skin; sweating or chills; nausea, diarrhea, belching, gas; muscle pain, leg cramps; or sleep problems (insomnia). This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. Side Effects (complete list) What other drugs will affect B3-500-Gr (niacin)? Tell your doctor about all other cholesterol-lowering drugs you are taking with niacin, especially atorvastatin (Lipitor, Caduet), fluvastatin (Lescol), lovastatin (Mevacor, Altoprev, Advicor), pravastatin (Pravachol), or simvastatin (Zocor, Simcor, Vytorin, Juvisync). Ask a doctor or pharmacist if it is safe for you to use niacin if you are also using any of the following drugs: a blood thinner such as warfarin (Coumadin, Jantoven); multivitamins or mineral supplements that contain niacin; blood pressure or heart medications such as amlodipine (Norvasc, Caduet, Exforge, Lotrel, Tekamlo, Tribenzor, Twynsta, Amturnide), diltiazem (Cardizem, Cartia, Dilacor, Diltia, Diltzac, Taztia, Tiazac), felodipine (Plendil), nicardipine (Cardene), nifedipine (Procardia, Adalat), nimodipine (Nimotop), nisoldipine (Sular), or verapamil (Calan, Covera, Isoptin, Verelan); or heart medications such as doxazosin (Cardura), isosorbide (Dilatrate, Imdur, Isordil, Monoket, Sorbitrate), nitroglycerin (Nitro-Bid, Nitro-Dur, Nitrostat), prazosin (Minipress), or terazosin (Hytrin). This list is not complete and other drugs may interact with niacin. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor. Next Side Effects Print this page Add to My Med List More about B3-500-Gr (niacin) Side Effects During Pregnancy Dosage Information Drug Interactions Support Group En Espaรฑol 1 Review Add your own review/rating Drug class: miscellaneous antihyperlipidemic agents Consumer resources Other brands: Niaspan , Niacor , Slo-Niacin , Niacin SR , ... +2 more Professional resources Niacin (AHFS Monograph) Niacin (FDA) Related treatment guides High Cholesterol Hyperlipoproteinemia Hyperlipoproteinemia Type IV, Elevated VLDL Hyperlipoproteinemia Type V, Elevated Chylomicrons VLDL Niacin Deficiency Pellagra Where can I get more information? Your pharmacist can provide more information about niacin. Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed. Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist. Copyright 1996-2012 Cerner Multum, Inc. Version: 8.04. Date modified: December 03, 2017 Last reviewed: May 15, 2012} Drug Status Rx OTC Availability Rx and/or OTC C Pregnancy Category Risk cannot be ruled out N/A CSA Schedule Not a controlled drug Drug Class Miscellaneous antihyperlipidemic agents Vitamins Related Drugs High Cholesterol atorvastatin , simvastatin , Crestor , Lipitor , Zocor , Zetia , More... Niacin Deficiency niacin , niacinamide , Niacor , Slo-Niacin , More... Hyperlipoproteinemia atorvastatin , simvastatin , Crestor , fenofibrate , Lipitor , pravastatin , More... Hyperlipoproteinemia Type IV, Elevated VLDL atorvastatin , simvastatin , Crestor , fenofibrate , Lipitor , pravastatin , More... 2 more conditions... B3-500-Gr Rating 1 User Review 9.0 /10 1 User Review 9.0 Rate it! Help and Support Looking for answers? Ask a question or go join the B3-500-Gr support group to connect with others who have similar interests.} } business enterprise


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the whole thing Babee Cof to flamable

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Photo :Babee Cof

the plain Babee Cof Generic Name: dextromethorphan (DEX troe me THOR fan) Brand Name: Babee Cof, Benylin DM Pediatric, Buckleys Mixture, Creomulsion, DayQuil Cough, Delsym, Elixsure Cough, Father John's Medicine, Robafen Cough Liquidgels, Robitussin Honey Cough, Scot-Tussin Diabetic, Silphen DM, St. Joseph Cough Suppressant, Sucrets DM Cough, Triaminic Long Acting Cough Overview Side Effects Dosage Interactions Pregnancy More Breastfeeding Warnings User Reviews Support Group Q & A What is Babee Cof (dextromethorphan)? Dextromethorphan is a cough suppressant. It affects the signals in the brain that trigger cough reflex. Dextromethorphan is used to treat a cough. Dextromethorphan will not treat a cough that is caused by smoking, asthma, or emphysema. Dextromethorphan may also be used for purposes not listed in this medication guide. Slideshow Seasoned Pro: Be Mindful of These Winter Health Hazards What is the most important information I should know about Babee Cof (dextromethorphan)? Always ask a doctor before giving a cough or cold medicine to a child. Death can occur from the misuse of cough and cold medicines in very young children. Do not use dextromethorphan if you have used an MAO inhibitor in the past 14 days, such as isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, or tranylcypromine. What should I discuss with my healthcare provider before taking Babee Cof (dextromethorphan)? Do not use dextromethorphan if you have used an MAO inhibitor in the past 14 days. A dangerous drug interaction could occur. MAO inhibitors include isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, tranylcypromine, and others. Ask a doctor or pharmacist about using this medicine if you have emphysema or chronic bronchitis. It is not known whether dextromethorphan will harm an unborn baby. Do not use this medicine without a doctor's advice if you are pregnant. This medication may pass into breast milk and could harm a nursing baby. Do not use this medicine without a doctor's advice if you are breast-feeding a baby. Artificially sweetened liquid medicine may contain phenylalanine. Check the medication label if you have phenylketonuria (PKU). How should I take Babee Cof (dextromethorphan)? There are many brands and forms of dextromethorphan available. Not all brands are listed on this leaflet. Use this medication exactly as directed on the label, or as it has been prescribed by your doctor. Do not use the medication in larger amounts, or use it for longer than recommended. Cough medicine is usually taken only for a short time until your symptoms clear up. Do not give this medicine to a child younger than 4 years old. Always ask a doctor before giving a cough or cold medicine to a child of any age. Death can occur from the misuse of cough and cold medicines in very young children. Measure liquid medicine with the dosing syringe provided, or with a special dose-measuring spoon or medicine cup. If you do not have a dose-measuring device, ask your pharmacist for one. Drink extra fluids to help loosen the congestion and lubricate your throat while you are taking this medication. Talk with your doctor if your symptoms do not improve after 7 days of treatment, or if you have a fever with a headache, cough, or skin rash. If you need to have any type of surgery, tell the surgeon ahead of time if you have taken a cough medicine within the past few days. Store dextromethorphan at room temperature, away from heat, light, and moisture. What happens if I miss a dose? Since cough medicine is usually taken only as needed, you may not be on a dosing schedule. If you are taking the medication regularly, take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at your next regularly scheduled time. Do not take extra medicine to make up the missed dose. What happens if I overdose? Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. What should I avoid while taking Babee Cof (dextromethorphan)? Avoid drinking alcohol. It can increase some of the side effects of dextromethorphan. This medication can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid taking diet pills, caffeine pills, or other stimulants (such as ADHD medications) without your doctor's advice. Taking a stimulant together with cough medicine can increase your risk of unpleasant side effects. Ask a doctor or pharmacist before using any cold, allergy, or pain medication. Many medicines available over the counter contain dextromethorphan. Taking certain products together can cause you to get too much of this type of medication. Check the label to see if a medicine contains a cough suppressant. Babee Cof (dextromethorphan) side effects Get emergency medical help if you have signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop using dextromethorphan and call your doctor at once if you have: severe dizziness, anxiety, restless feeling, or nervousness; confusion, hallucinations; or slow, shallow breathing. Common side effects may include stomach upset. This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. Side Effects (complete list) What other drugs will affect Babee Cof (dextromethorphan)? Ask a doctor or pharmacist before using this medicine if you are also using any other drugs, including prescription and over-the-counter medicines, vitamins, and herbal products. Some medicines can cause unwanted or dangerous effects when used together. Not all possible interactions are listed in this medication guide. Taking this medicine with other drugs that make you sleepy or slow your breathing can worsen these effects. Ask your doctor before taking dextromethorphan with a sleeping pill, narcotic pain medicine, muscle relaxer, or medicine for anxiety, depression, or seizures. Next Side Effects Print this page Add to My Med List More about Babee Cof (dextromethorphan) Side Effects During Pregnancy or Breastfeeding Dosage Information Drug Interactions Support Group En Espaรฑol 0 Reviews Add your own review/rating Drug class: antitussives Consumer resources Babee Cof Syrup (Advanced Reading) Other brands: Delsym , DexAlone , St. Joseph Cough Suppressant , Vicks Dayquil Cough , ... +13 more Professional resources Dextromethorphan Hydrobromide (AHFS Monograph) Related treatment guides Cough Where can I get more information? Your pharmacist can provide more information about dextromethorphan. Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed. Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist. Copyright 1996-2012 Cerner Multum, Inc. Version: 7.01. Date modified: December 03, 2017 Last reviewed: February 09, 2016} Drug Status Rx OTC Availability Rx and/or OTC C Pregnancy Category Risk cannot be ruled out N/A CSA Schedule Not a controlled drug Drug Class Antitussives Related Drugs Cough benzonatate , acetaminophen / hydrocodone , diphenhydramine , Benadryl , Mucinex , guaifenesin , Dilaudid , Promethazine DM , hydromorphone , Lortab , codeine , Tessalon Perles , Tessalon , Cheratussin AC , dextromethorphan , Tylenol with Codeine #3 , Mucinex DM , acetaminophen / codeine , codeine / guaifenesin , Tylenol with Codeine , Hydromet , Tussionex Pennkinetic , More... Babee Cof Rating No Reviews - Be the first! No Reviews - Be the first! Not Rated - Be the first! Help and Support Looking for answers? Ask a question or go join the Babee Cof support group to connect with others who have similar interests.} } and you are going


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wake-up call B-Tuss in a well mannered way

wake-up call B-Tuss in a well mannered way

most unlikely B-Tuss sizeable
 
Photo :B-Tuss

is unnecessary B-Tuss Generic Name: chlorpheniramine, hydrocodone, and phenylephrine (KLOR fe NEER a meen, HYE droe KOE done, FEN il EFF rin) Brand Name: B-Tuss, De-Chlor HC, DroTuss-CP, Hydron CP, Hydro-PC II, Poly-Tussin HD, Relasin-HC, Triant-HC, Z-Cof HC Overview Side Effects Dosage Interactions Pregnancy More User Reviews Support Group Q & A What is B-Tuss (chlorpheniramine, hydrocodone, and phenylephrine)? Chlorpheniramine is an antihistamine that reduces the natural chemical histamine in the body. Histamine can produce symptoms of sneezing, itching, watery eyes, and runny nose. Hydrocodone is a narcotic cough medicine. Phenylephrine is a decongestant that shrinks blood vessels in the nasal passages. Dilated blood vessels can cause nasal congestion (stuffy nose). Chlorpheniramine, hydrocodone, and phenylephrine is a combination medicine used to treat runny or stuffy nose, sinus congestion, and cough caused by the common cold or flu. Chlorpheniramine, hydrocodone, and phenylephrine may also be used for purposes not listed in this medication guide. Slideshow OTC Medication Use In Pregnancy: Wise or Worrisome? What is the most important information I should know about this medicine? Do not use this medicine if you have used an MAO inhibitor in the past 14 days, such as isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, or tranylcypromine. You should not use this medicine if you have recently used alcohol, sedatives, tranquilizers, or other narcotic medications. What should I discuss with my healthcare provider before taking this medicine? Do not use this medicine if you have taken an MAO inhibitor in the past 14 days. A dangerous drug interaction could occur. MAO inhibitors include isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, and tranylcypromine. You should not use chlorpheniramine, hydrocodone, and phenylephrine if you are allergic to it, or if you have recently used alcohol, sedatives, tranquilizers, or other narcotic medications. To make sure this medicine is safe for you, tell your doctor if you have: blockage in your digestive tract (stomach or intestines); diarrhea, inflammatory bowel disease; a colostomy or ileostomy; liver or kidney disease; heart disease; glaucoma; bladder obstruction or other urination problems; a head injury or brain tumor; asthma, COPD, sleep apnea, or other breathing disorder; a thyroid disorder; pheochromocytoma (tumor of the adrenal gland); low blood pressure; or if you are dehydrated. It is not known whether this medicine will harm an unborn baby. If you use hydrocodone while you are pregnant, your baby could become dependent on the drug. This can cause life-threatening withdrawal symptoms in the baby after it is born. Babies born dependent on habit-forming medicine may need medical treatment for several weeks. Tell your doctor if you are pregnant or plan to become pregnant. Chlorpheniramine, hydrocodone, and phenylephrine can pass into breast milk and may harm a nursing baby. You should not breast-feed while using this medicine. How should I take this medicine? Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended. Hydrocodone may be habit-forming. Never share this medicine with another person, especially someone with a history of drug abuse or addiction. Keep the medication in a place where others cannot get to it. Selling or giving away this medicine is against the law. Misuse of habit-forming medicine can cause addiction, overdose, or death. Selling or giving away this medicine is against the law. You may take this medication with or without food. Measure liquid medicine with the dosing syringe provided, or with a special dose-measuring spoon or medicine cup. If you do not have a dose-measuring device, ask your pharmacist for one. Store at room temperature away from moisture and heat. Keep track of the amount of medicine used from each new bottle. Hydrocodone is a drug of abuse and you should be aware if anyone is using your medicine improperly or without a prescription. What happens if I miss a dose? Since this medicine is used when needed, you may not be on a dosing schedule. If you are on a schedule, use the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not use extra medicine to make up the missed dose. What happens if I overdose? Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose of hydrocodone can be fatal. Overdose symptoms may include extreme drowsiness, pinpoint pupils, confusion, cold and clammy skin, weak pulse, shallow breathing, fainting, or breathing that stops. What should I avoid while taking this medicine? This medication may cause blurred vision and may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert and able to see clearly. Drinking alcohol can increase certain side effects of chlorpheniramine, hydrocodone, and phenylephrine. This medicine side effects Get emergency medical help if you have signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop using this medicine and call your doctor at once if you have: pounding heartbeats or fluttering in your chest; a light-headed feeling, like you might pass out; severe anxiety, confusion, fear; painful or difficult urination; little or no urinating; or dangerously high blood pressure--severe headache, blurred vision, pounding in your neck or ears, nosebleed, anxiety, confusion, severe chest pain, shortness of breath, irregular heartbeats. Side effects such as dry mouth, constipation, and confusion may be more likely in older adults. Common side effects may include: dizziness, drowsiness; mood changes; blurred vision; or nausea, vomiting. This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. Side Effects (complete list) What other drugs will affect this medicine? Taking this medicine with other drugs that make you sleepy or slow your breathing can cause dangerous or life-threatening side effects. Ask your doctor before taking chlorpheniramine, hydrocodone, and phenylephrine with a sleeping pill, narcotic pain medicine, muscle relaxer, or medicine for anxiety, depression, or seizures. Other drugs may interact with chlorpheniramine, hydrocodone, and phenylephrine, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell each of your health care providers about all medicines you use now and any medicine you start or stop using. Next Side Effects Print this page Add to My Med List More about B-Tuss (chlorpheniramine / hydrocodone / phenylephrine) Side Effects During Pregnancy Dosage Information Drug Interactions Support Group En Espaรฑol 0 Reviews Add your own review/rating Drug class: upper respiratory combinations Consumer resources Other brands: Relasin-HC , Triant-HC , Hydro-PC II , De-Chlor HC , ... +4 more Related treatment guides Cough and Nasal Congestion Where can I get more information? Your pharmacist can provide more information about chlorpheniramine, hydrocodone, and phenylephrine. Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed. Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist. Copyright 1996-2012 Cerner Multum, Inc. Version: 6.02. Date modified: December 03, 2017 Last reviewed: August 10, 2016} Drug Status Rx Availability Prescription only C Pregnancy Category Risk cannot be ruled out 2 CSA Schedule High potential for abuse WADA Class Anti-Doping Classification Drug Class Upper respiratory combinations Related Drugs Cough and Nasal Congestion Promethazine VC with Codeine , Bromfed DM , Mucinex D , Vanacof , Deconex , codeine / phenylephrine / promethazine , Resperal-DM , Vicks NyQuil Severe Cold & Flu , Vicks Nyquil Cough , Coricidin HBP Cough & Cold , Deconex DMX , Crantex , Tussin CF , Robitussin Allergy & Cough , Robitussin Nighttime Cough DM , Mucinex Fast-Max Severe Congestion & Cough , Relasin-HC , Dimetapp Children's Cold & Cough , More... B-Tuss Rating No Reviews - Be the first! No Reviews - Be the first! Not Rated - Be the first! Help and Support Looking for answers? Ask a question or go join the B-Tuss support group to connect with others who have similar interests.} } concept


very unlikely B-Tuss that i wonder
of issues of safety B-Nexa Tablets cost

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a chronic B-Nexa Tablets is legendary
 
Photo :B-Nexa Tablets

to picking B-Nexa Tablets Generic Name: pyridoxine, folic acid, calcium, and ginger Dosage Form: tablet Overview Side Effects Dosage Professional Interactions More User Reviews Drug Images Support Group Q & A Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here. B-NEXA TABLETS Rx only B-Nexa Tablets Description B-Nexa Tablets are a prescription prenatal vitamin that provide B-vitamin nutrition and are formulated with vitamin B 6 and ginger to help calm nausea and vomiting of pregnancy (NVP). B-Nexa Tablets contain 100 mg ginger root powder extract that, when standardized to gingerols, is equivalent to 500 mg ginger root powder. Each caplet shaped tablet is engraved "US" on one side and "214" on the other with a pink film coat. Each pink tablet contains: Vitamin B 6 (pyridoxine hydrochloride, USP) 40 mg Folic Acid, USP 1.2 mg Calcium (as dicalcium phosphate and tricalcium phosphate) 124.1 mg Ginger (zingiber officinale) root powder extract 100 mg Other Ingredients: microcrystalline cellulose, maltodextrin, talc, corn starch, croscarmellose sodium, stearic acid, hypromellose, hydroxypropyl cellulose, magnesium stearate, silicon dioxide, titanium dioxide, iron oxide red, iron oxide yellow, iron oxide black. Slideshow OTC Medication Use In Pregnancy: Wise or Worrisome? INDICATIONS B-Nexa Tablets are indicated to provide B-vitamin supplementation, with ginger to help calm pregnancy related nausea and vomiting (morning sickness), and may be used in conjunction with a physician prescribed prenatal regimen. Contraindications This product is contraindicated in patients with a known hypersensitivity to any of the ingredients. Precautions Folic acid alone is improper therapy in the treatment of pernicious anemia and other megaloblastic anemias where vitamin B 12 is deficient. Folic acid in doses above 1 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations progress. Concomitant use of ginger in patients with bleeding disorders, or who are on anti-coagulant or anti-platelet therapy, may increase the risk of bleeding. Adverse Reactions Allergic sensitization has been reported following both oral and parenteral administration of folic acid. B-Nexa Tablets Dosage and Administration One or two tablets daily, in divided doses, or as directed by a physician. How is B-Nexa Tablets Supplied Bottles of 60 tablets (NDC 0245-0214-60). KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN. DO NOT CHEW Store at controlled room temperature, 15-30°C (59-86°F). Protect from light and moisture. Distributed by: UPSHER-SMITH LABORATORIES, INC. 6701 Evenstad Drive Maple Grove, MN 55369 1-800-654-2299 www.upsher-smith.com 104472-06 Revised 0911 PRINCIPAL DISPLAY PANEL - 60 Tablet Bottle Label NDC 0245-0214-60 Rx ONLY NEW! TABLETS B-Nexa Rx PRENATAL VITAMIN WITH B VITAMINS AND GINGER UNIQUELY FORMULATED WITH VITAMIN B 6 AND GINGER TO HELP CALM NAUSEA AND VOMITING OF PREGNANCY (NVP) 60 TABLETS B-NEXA pyridoxine, folic acid, calcium, and ginger tablet Product Information Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0245-0214 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Pyridoxine (Pyridoxine) Pyridoxine 40 mg Folic Acid (Folic Acid) Folic Acid 1.2 mg Calcium (Calcium) Calcium 124.1 mg Ginger (Ginger) Ginger 100 mg Inactive Ingredients Ingredient Name Strength Cellulose, Microcrystalline Maltodextrin Talc Starch, Corn Croscarmellose Sodium Stearic Acid Hypromelloses Silicon Dioxide Titanium Dioxide Hydroxypropyl Cellulose Magnesium Stearate Ferrosoferric Oxide Ferric Oxide Yellow Ferric Oxide Red Product Characteristics Color PINK Score no score Shape OVAL Size 24mm Flavor Imprint Code US;214 Contains Packaging # Item Code Package Description 1 NDC:0245-0214-60 60 TABLET (TABLET) in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 12/08/2011 Labeler - Upsher-Smith Laboratories, Inc. (047251004) Establishment Name Address ID/FEI Operations Upsher-Smith Laboratories, Inc. 047251004 ANALYSIS Establishment Name Address ID/FEI Operations Accucaps Industries Limited 248441727 ANALYSIS, MANUFACTURE Revised: 12/2011 Upsher-Smith Laboratories, Inc. Next Interactions Print this page Add to My Med List More about B-Nexa (calcium / folic acid / ginger / pyridoxine) Side Effects Dosage Information Drug Images Drug Interactions Support Group 0 Reviews Add your own review/rating Drug class: vitamin and mineral combinations Consumer resources B-Nexa Professional resources Other brands: Zingiber , Focalgin-B Related treatment guides Nausea/Vomiting of Pregnancy FEATURED: CAR-T Cell Therapy Overview Mechanism of Action KTE-C19 Studies KTE-C19 Cancer Targets Adverse Events Manufacturing Drug Status Rx Availability Prescription only N Pregnancy Category Not classified N/A CSA Schedule Not a controlled drug Manufacturer Upsher-Smith Laboratories Inc. Drug Class Vitamin and mineral combinations Related Drugs vitamin and mineral combinations multivitamin , Citracal + D Nausea / Vomiting of Pregnancy Diclegis , calcium / folic acid / ginger / pyridoxine , doxylamine / pyridoxine , Zingiber , Bonjesta , More... B-Nexa Rating No Reviews - Be the first! No Reviews - Be the first! Not Rated - Be the first! B-Nexa Images B-Nexa Prenatal Multivitamins with Folic Acid 1.22 mg (US 215) View larger images sizable of style


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