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Photo :SLEEP-TITE (Wellness International) Herbal Sleep Aid
apart from SLEEP-TITE (Wellness International) Herbal Sleep Aid Uses: Sleep-Tite is a non-addicting herbal sleep aid formulated to promote a deeper, more restorative sleep without the use of pharmaceutically synthesized hormones. With the body's overall health, and proper functioning, dependent upon efficient sleep patterns in order to achieve cellular, organ, tissue and emotional repair, this powerful tool's primary function is to rejuvenate and restore by assisting the body in initiating and maintaining sleep. Sleep-Tite is a blend of 10 highly effective, all-natural herbs. California poppy, passion flower, valerian, kava kava and skullcap have been used for centuries as a remedy for insomnia because of their calming effects and ability to relieve muscle tension. Hops and celery seed produce a generalized calming effect and are especially helpful for indigestion, gastrointestinal and smooth muscle relaxation. Chamomile also has a relaxing effect on the body and the gastrointestinal tract, but with the added benefit of producing anti-inflammatory effects on joints. Feverfew has been used as a treatment for fever, migraines and arthritic complaints dating back to ancient Greece. A study published in Lancet demonstrated that feverfew inhibited the body's production of prostaglandin and serotonin. These biochemicals can cause inflammation, fever and the vasoactive response that triggers migraine headaches. By utilizing this unique blend of herbs to aid in the effective initiation and maintenance of sleep patterns, Sleep-Tite can be consumed by adults, thereby promoting physical and emotional well-being in a safe, active manner. Directions: Adults (18 years and older) may take two Sleep-Tite caplets approximately 30 to 60 minutes prior to bedtime. Needs may vary with each individual. Some persons may require less than two caplets to achieve optimum results. Do not exceed recommended nightly amounts. Warnings: Not for use by children, pregnant women or lactating women. Consult your physician before using this product if you have any medical condition or are taking antidepressant, sedative or hypnotic medications. Do not take this product if using Monoamine Oxidase Inhibitors (MAOI). This product may cause drowsiness and should not be taken with alcohol or while operating a vehicle or other machinery. If allergic symptoms develop, discontinue use. Store in a cool, dry place. Keep out of reach of children. Ingredients: European Valerian Root 4:1 extract, Celery Seed 4:1 extract, Hops Strobile 4:1 extract, Passion Flower 4:1 extract (whole plant), California Poppy 5:1 extract (aerial parts), Chamomile Flower 5:1 extract, Chinese Fu Ling 5:1 extract (Poria Cocos), Kava Kava Root 5:1 extract, Feverfew 5:1 extract (aerial parts), Skullcap (aerial parts), Dicalcium Phosphate, Microcrystalline Cellulose, Croscarmellose Sodium, Stearic Acid, Silica, Magnesium Stearate and Sugar Coat (calcium sulfate, sucrose, kaolin, talc, gelatin, shellac, titanium dioxide, anise oil, beeswax and carnauba wax). How Supplied One box contains 28 packets. Two caplets per packet. Print this page work at home


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Photo :Slo-Niacin
previous couple of Slo-Niacin 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 Drug Images Support Group Q & A What is Slo-Niacin (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 Slo-Niacin (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 Slo-Niacin (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 Slo-Niacin (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 Slo-Niacin (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. Slo-Niacin (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 Slo-Niacin (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 Slo-Niacin (niacin) Side Effects During Pregnancy Dosage Information Drug Images Drug Interactions Support Group En Español 2 Reviews Add your own review/rating Drug class: miscellaneous antihyperlipidemic agents Consumer resources Slo-Niacin Slo-Niacin (Advanced Reading) Other brands: Niaspan , Niacor , Niacin SR , Nicotinex , ... +2 more Professional resources Niacin (AHFS Monograph) Niacin (FDA) Related treatment guides High Cholesterol Pellagra Hyperlipoproteinemia Hyperlipoproteinemia Type IV, Elevated VLDL Hyperlipoproteinemia Type V, Elevated Chylomicrons VLDL Niacin Deficiency 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 , Nicotinex , More... Hyperlipoproteinemia atorvastatin , simvastatin , Crestor , fenofibrate , Lipitor , pravastatin , More... Hyperlipoproteinemia Type IV, Elevated VLDL atorvastatin , simvastatin , Crestor , fenofibrate , Lipitor , pravastatin , More... 2 more conditions... Slo-Niacin Rating 2 User Reviews 9.5 /10 2 User Reviews 9.5 Rate it! Slo-Niacin Images Slo-Niacin 250 MG (250 ) View all images Related Questions & Answers What if my husband opens the Slo-Niacin capsule to take it? Hi, Can I find another niacin without hydrogenated oil in it as in Slo-Niacin Polygel Niacin? What is the basic difference in Slo-Niacin and Niaspan? I have been taking Niaspan for several months with good results? I've been taking Slo-Niacin for 2months,and wanting to know if Slo-Niacin flushes out your system? Read more questions} } finest


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Photo :Sleepinal
actually Sleepinal Generic Name: diphenhydramine (DYE fen HYE dra meen) Brand Name: Allergy Relief (Diphenhydramine HCl), Allermax, Banophen, Benadryl, Compoz Nighttime Sleep Aid, Diphedryl, Diphenhist, Dytuss, Nytol QuickCaps, PediaCare Children's Allergy, Q-Dryl, QlearQuil Nightitme Allergy Relief, Quenalin, Scot-Tussin Allergy Relief Formula, Siladryl Allergy, Silphen Cough, Simply Sleep, Sleepinal, Sominex, Tranquil, Twilite, Unisom Sleepgels Maximum Strength, Valu-Dryl, Vanamine PD, Z-Sleep, ZzzQuil Overview Side Effects Dosage Interactions Pregnancy More Breastfeeding Warnings User Reviews Support Group Q & A What is Sleepinal (diphenhydramine)? Diphenhydramine is an antihistamine that reduces the effects of natural chemical histamine in the body. Histamine can produce symptoms of sneezing, itching, watery eyes, and runny nose. Diphenhydramine is used to treat sneezing, runny nose, watery eyes, hives, skin rash, itching, and other cold or allergy symptoms. Diphenhydramine is also used to treat motion sickness, to induce sleep, and to treat certain symptoms of Parkinson's disease. Diphenhydramine may also be used for purposes not listed in this medication guide. Slideshow View Frightful (But Dead Serious) Drug Side Effects What is the most important information I should know about Sleepinal (diphenhydramine)? You should not use antihistamine medication to make a child sleepy. What should I discuss with my healthcare provider before taking Sleepinal (diphenhydramine)? You should not use diphenhydramine if you are allergic to it. Ask a doctor or pharmacist if it is safe for you to take this medicine if you have other medical conditions, especially: blockage in your digestive tract (stomach or intestines); bladder obstruction or other urination problems; a colostomy or ileostomy; liver or kidney disease; asthma, chronic obstructive pulmonary disease (COPD), or other breathing disorder; cough with mucus, or cough caused by smoking, emphysema, or chronic bronchitis; heart disease, low blood pressure; glaucoma; a thyroid disorder; or if you take potassium (Cytra, Epiklor, K-Lyte, K-Phos, Kaon, Klor-Con, Polycitra, Urocit-K). It is not known whether diphenhydramine will harm an unborn baby. Ask a doctor before using this medicine if you are pregnant. Diphenhydramine can pass into breast milk and may harm a nursing baby. Antihistamines may also slow breast milk production. Ask a doctor before using this medicine if you are breast-feeding. Older adults may be more likely to have side effects from this medicine. How should I take Sleepinal (diphenhydramine)? 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. Cold or allergy medicine is usually taken only for a short time until your symptoms clear up. Do not give this medication to a child younger than 2 years old. 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. You should not use antihistamine medication to make a child sleepy. 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. For motion sickness, take diphenhydramine 30 minutes before you will be in a situation that causes you motion sickness (such as a long car ride, airplane or boat travel, amusement park rides, etc). Continue taking diphenhydramine with meals and at bedtime for the rest of the time you will be in a motion-sickness situation. As a sleep aid, take diphenhydramine within 30 minutes before bedtime. Call 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. This medication can affect the results of allergy skin tests. Tell any doctor who treats you that you are using diphenhydramine. Store at room temperature away from moisture and heat. What happens if I miss a dose? Since diphenhydramine 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. What should I avoid while taking Sleepinal (diphenhydramine)? 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 diphenhydramine. Ask a doctor or pharmacist before using any other cold, cough, allergy, or sleep medicine. Antihistamines are contained in many combination medicines. Taking certain products together can cause you to get too much of this type of medicine. Check the label to see if a medicine contains an antihistamine. Sleepinal (diphenhydramine) side effects 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 diphenhydramine and call your doctor at once if you have: pounding heartbeats or fluttering in your chest; painful or difficult urination; little or no urinating; confusion, feeling like you might pass out; or tightness in your neck or jaw, uncontrollable movements of your tongue. Common side effects may include: dizziness, drowsiness, loss of coordination; dry mouth, nose, or throat; constipation, upset stomach; dry eyes, blurred vision; or day-time drowsiness or "hangover" feeling after night-time use. 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 Sleepinal (diphenhydramine)? 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 diphenhydramine 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 Sleepinal (diphenhydramine) Side Effects During Pregnancy or Breastfeeding Dosage Information Drug Interactions Support Group En Español 0 Reviews Add your own review/rating Drug class: anticholinergic antiemetics Consumer resources Other brands: Benadryl , Banophen , Benadryl Allergy , ZzzQuil , ... +25 more Professional resources Diphenhydramine Hydrochloride (AHFS Monograph) Diphenhydramine Oral Solution (FDA) Related treatment guides Insomnia Where can I get more information? Your pharmacist can provide more information about diphenhydramine. 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: 6.01. Date modified: December 03, 2017 Last reviewed: April 17, 2017} Drug Status Rx OTC Availability Rx and/or OTC B Pregnancy Category No proven risk in humans N/A CSA Schedule Not a controlled drug Drug Class Anticholinergic antiemetics Anticholinergic antiparkinson agents Antihistamines Miscellaneous anxiolytics, sedatives and hypnotics Related Drugs Insomnia melatonin , lorazepam , zolpidem , amitriptyline , Ambien , temazepam , Ativan , diphenhydramine , doxepin , Elavil , Restoril , Ibuprofen PM , Belsomra , Lunesta , eszopiclone , Rozerem , triazolam , zaleplon , doxylamine , Sonata , Silenor , Halcion , flurazepam , ramelteon , More... Sleepinal Rating No Reviews - Be the first! No Reviews - Be the first! Not Rated - Be the first! Related Questions & Answers Sleep Disorders - I have trouble sleeping that's why I am awake now on line, I want to sleep but I? Read more questions} } that supply


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Photo :Baci-IM (injection)
that offer Baci-IM (injection) Generic Name: bacitracin (injection) (BAS i TRAY sin) Brand Name: Baci-IM Overview Side Effects Dosage Professional Interactions More Breastfeeding Warnings User Reviews Support Group Q & A What is Baci-IM (bacitracin injection)? Bacitracin injection is an antibiotic that treats staph infection caused by a bacteria called staphylococcus (STAF-il-oh-KOK-us). Bacitracin injection is used in infants to treat pneumonia. It is also used to treat an infection that causes pus to build up between the lungs and the membrane that covers them. Bacitracin injection may also be used for purposes not listed in this medication guide. Slideshow The Shocking Truth About Antibiotic Resistance What is the most important information I should know about Baci-IM (bacitracin injection)? Bacitracin can harm your baby's kidneys. This effect is increased when the baby also uses certain other medicines, especially injected antibiotics. Your baby's kidney function will need to be tested before and during treatment with bacitracin. What should I discuss with my health care provider before receiving Baci-IM (bacitracin injection)? Your baby should not receive this medicine if he or she is allergic to bacitracin. To make sure bacitracin is safe for your baby, tell the doctor if your baby has: kidney disease; or any known allergies. How is Baci-IM (bacitracin injection) given? Bacitracin is injected into a muscle. A healthcare provider will give your baby this injection. Lung infections in infants are serious conditions, and your baby will most likely be kept in the hospital while being treated with bacitracin injection. While receiving bacitracin, your baby's kidney function will need to be tested daily. Make sure your baby receives this medicine for the full prescribed length of time. Symptoms may improve before the infection is completely cleared. Skipping doses may also increase the risk of further infection that is resistant to antibiotics. Bacitracin will not treat a viral infection such as the flu or a common cold. What happens if I miss a dose? Because your child will receive bacitracin in a clinical setting, he or she is not likely to miss a dose. What happens if I overdose? Since this medicine is given by a healthcare professional in a medical setting, an overdose is unlikely to occur. What should I avoid while receiving Baci-IM (bacitracin injection)? Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If your baby has diarrhea that is watery or bloody, call your doctor. Do not give your baby anti-diarrhea medicine unless your doctor tells you to. Baci-IM (bacitracin injection) side effects Get emergency medical help if your baby has any of these signs of an allergic reaction: hives; difficult breathing; swelling of the face, lips, tongue, or throat. While receiving bacitracin injection, your baby will be watched for the following side effects: diarrhea that is watery or bloody; urinating more than usual or more often; little or no urinating (fewer wet diapers); blood in the urine; lower back pain; or painful urination. Common side effects include: nausea, vomiting; mild skin rash; or pain, burning, or swelling where the medicine was injected. This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088. Side Effects (complete list) What other drugs will affect Baci-IM (bacitracin injection)? Bacitracin can harm your baby's kidneys. This effect is increased when the baby also receives certain other medicines. Tell your doctor about all medicines your baby uses, especially: antivirals; chemotherapy; injected antibiotics; medicine for bowel disorders; medicine to prevent organ transplant rejection; or some pain or arthritis medicines (including aspirin, Tylenol, Advil, and Aleve). This list is not complete. Other drugs may interact with bacitracin, including prescription and over-the-counter medicines, vitamins, and herbal products. Not all possible interactions are listed in this medication guide. Next Side Effects Print this page Add to My Med List More about BACiiM (bacitracin) Side Effects Breastfeeding Dosage Information Drug Interactions Support Group En Español 0 Reviews Add your own review/rating Drug class: miscellaneous antibiotics Consumer resources BACiiM Professional resources BACiiM (AHFS Monograph) BACiiM (FDA) Related treatment guides Pneumonia Where can I get more information? Your doctor or pharmacist can provide more information about bacitracin injection. 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: 2.01. Date modified: December 03, 2017 Last reviewed: October 06, 2014 Drug Status Rx Availability Prescription only C Pregnancy Category Risk cannot be ruled out N/A CSA Schedule Not a controlled drug Approval History Drug history at FDA Drug Class Miscellaneous antibiotics Related Drugs Pneumonia ciprofloxacin , amoxicillin , azithromycin , doxycycline , metronidazole , Augmentin , Zithromax , Levaquin , levofloxacin , clindamycin , Bactrim , sulfamethoxazole / trimethoprim , cefdinir , ceftriaxone , Flagyl , vancomycin , cefuroxime , erythromycin , Rocephin , Ceftin , gentamicin , clarithromycin , amoxicillin / clavulanate , More... BACiiM 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 BACiiM support group to connect with others who have similar interests. among the best


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Photo :BACiiM
imaginable [5000:<2.5 kg: Manufacturers recommend 900 units/kg daily given in 2 or 3 divided doses. 100 104 Infants >2.5 kg: Manufacturers recommend 1000 units/kg daily in 2 or 3 divided doses. 100 104 Prescribing Limits Pediatric Patients Staphylococcal Pneumonia and Empyema in Infants Do not exceed recommended dosage; 100 104 duration >12 days not recommended. a Special Populations No special population dosage recommendations. 100 104 Cautions for BACiiM Contraindications History of hypersensitivity or toxic reactions to bacitracin. 100 104 Warnings/Precautions Warnings Nephrotoxicity IM bacitracin may cause renal failure due to tubular and glomerular necrosis. 100 104 Albuminuria, 100 104 hematuria, a cylindruria, 100 104 and rising blood concentrations of the drug 100 104 may occur initially followed eventually by oliguria, a azotemia, 100 104 and renal failure. 100 104 Infants less prone to bacitracin nephrotoxicity than older children and adults. a Toxicity is related to total daily dosage and duration of therapy. a Assess renal function prior to and daily during therapy. 100 104 Discontinue drug if renal toxicity occurs. 100 104 Keep patient well hydrated using oral or, if necessary, parenteral fluids. 100 104 Maintain urine output at proper levels to avoid renal toxicity. 100 104 Some suggest using sodium bicarbonate or another alkali to keep urine at pH 6 or greater to avoid renal irritation. a Avoid concomitant use with other nephrotoxic drugs. 100 104 (See Specific Drugs under Interactions.) Because of the risk of nephrotoxicity, manufacturers state restrict use of IM bacitracin only to the treatment of staphylococcal pneumonia and empyema in infants when the causative organism has been shown to be susceptible to the drug. 100 104 In addition, use the drug only if adequate laboratory facilities are available and constant supervision of the patient is possible. 100 104 Sensitivity Reactions Hypersensitivity Anaphylaxis and/or allergic contact dermatitis reported when bacitracin used for non-FDA-labeled indications. 100 104 Rash 100 104 and pruritus a also reported. General Precautions Superinfection/Clostridium difficile-associated Diarrhea and Colitis (CDAD) Possible emergence and overgrowth of nonsusceptible bacteria or fungi may occur. 100 104 Institute appropriate therapy if superinfection occurs. 100 104 Treatment with anti-infectives alters normal colon flora and may permit overgrowth of Clostridium difficile . 100 104 110 111 112 C. difficile infection (CDI) and CDAD (also known as antibiotic-associated diarrhea and colitis or pseudomembranous colitis) reported with nearly all anti-infectives and may range in severity from mild diarrhea to fatal colitis. 100 104 110 111 112 C. difficile produces toxins A and B which contribute to development of CDAD; 100 104 110 hypertoxin-producing strains of C. difficile are associated with increased morbidity and mortality since they may be refractory to anti-infectives and colectomy may be required. 100 104 Consider CDAD if diarrhea develops during or after therapy and manage accordingly. 100 104 110 111 112 Obtain careful medical history since CDAD may occur as late as ≥2 months after anti-infective therapy is discontinued. 100 104 If CDAD suspected or confirmed, discontinue anti-infectives not directed against C. difficile whenever possible. 100 104 110 Initiate appropriate supportive therapy (e.g., fluid and electrolyte management, protein supplementation), anti-infective therapy directed against C. difficile (e.g., metronidazole, vancomycin), and surgical evaluation as clinically indicated. 100 104 110 111 112 Selection and Use of Anti-infectives To reduce development of drug-resistant bacteria and maintain effectiveness of bacitracin and other antibacterials, use only for treatment or prevention of infections proven or strongly suspected to be caused by susceptible bacteria. 100 104 When selecting or modifying anti-infective therapy, use results of culture and in vitro susceptibility testing. 100 104 In the absence of such data, consider local epidemiology and susceptibility patterns when selecting anti-infectives for empiric therapy. 100 104 Specific Populations Pregnancy Category C. 145 Not labeled for use in adults, including pregnant women. 100 104 Lactation Not known whether bacitracin is distributed into milk. 145 Not labeled for use in adults, including nursing women. 100 104 Common Adverse Effects Nephrotoxicity (albuminuria, cylindruria, azotemia, rising blood concentrations of the drug); 100 104 GI effects (nausea, vomiting); 100 104 pain at injection site; 100 104 hypersensitivity reactions (rash). 100 104 Interactions for BACiiM Specific Drugs Drug Interaction Comments Aminoglycosides (kanamycin, neomycin, streptomycin) Possible additive nephrotoxic effects 14 Avoid concomitant use 14 100 104 Colistimethate/colistin Possible additive nephrotoxic effects 14 Avoid concomitant use 14 100 104 Polymyxin b sulfate Possible additive nephrotoxic effects 14 100 104 Avoid concomitant use 14 100 104 Neuromuscular blocking agents and general anesthetics Possible enhanced neuromuscular blockade if bacitracin used concomitantly during surgery or postoperatively 14 Vancomycin Possible additive nephrotoxic effects 14 Avoid concomitant use 14 100 BACiiM Pharmacokinetics Absorption Bioavailability Not appreciably absorbed from GI tract. 14 Completely and rapidly absorbed following IM injection. 100 104 Following IM dosage of 200 300 units/kg every 6 hours in individuals with normal renal function, serum concentrations are 0.2 2 mcg/mL. 100 104 Following single IM dose of 10,000 20,000 units in adults with normal renal function, peak serum concentrations occur after 1 2 hours and the drug is detectable in serum for 6 8 hours after the dose. a Distribution Extent Widely distributed into all body organs; 100 104 readily diffuses into ascitic and pleural fluids following IM injection. 100 104 Only low concentrations distributed into CSF. 14 Plasma Protein Binding Only slightly protein bound. a Elimination Elimination Route IM: 10 40% of a dose excreted slowly by glomerular filtration and appears in urine within 24 hours. 14 Oral: Excreted in feces. a Stability Storage Parenteral Powder for Injection 2 8°C. 100 104 Following reconstitution with 0.9% sodium chloride injection containing 2% procaine hydrochloride as directed by manufacturer, stable at 2 8°C for 1 week. 100 104 Actions and Spectrum Polypeptide antibiotic produced by B. subtilis or B. licheniformis ; 7 14 100 104 bacitracin commercially available in US is derived from cultures of B. subtilis (Tracey). 100 104 Mixture of polypeptides (bacitracin A, B1, B2, B3); 7 100 104 major component is bacitracin A. 100 104 Commercially available bacitracin for injection has a potency of not less than 50 units of bacitracin activity per mg. 7 100 104 May be bactericidal or bacteriostatic, depending on drug concentration at site of infection. a Inhibits bacterial cell wall synthesis. a Active in vitro against some gram-positive bacteria, including staphylococci (e.g., Staphylococcus aureus ) and Streptococcus pyogenes (group A β-hemolytic streptococci, GAS). 144 Also active in vitro against some gram-negative bacteria, including Haemophilus influenzae and Neisseria , but not active against most gram-negative bacilli. 14 144 Although some strains of Clostridium difficile are susceptible to bacitracin in vitro, 142 strains with high-level resistance to the drug reported. 113 141 142 144 S. aureus resistant to bacitracin have been reported. 14 144 Does not exhibit cross-resistance with other antibiotics. a Advice to Patients Advise patients that antibacterials (including bacitracin) should only be used to treat bacterial infections and not used to treat viral infections (e.g., the common cold). 100 104 Advise patients that it is common to begin feeling better after a few days, but that skipping doses or not completing the full course of therapy may decrease effectiveness and increase the likelihood that bacteria will develop resistance and will not be treatable with bacitracin or other antibacterials in the future. 100 104 Advise patients that diarrhea is a common problem caused by anti-infectives and usually ends when the drug is discontinued. 100 104 Importance of contacting a clinician if watery and bloody stools (with or without stomach cramps and fever) occur during or as late as 2 months or longer after the last dose. 100 104 Importance of informing clinicians of existing concomitant therapy, including prescription and OTC drugs, as well as any concomitant illnesses. 100 104 Importance of informing patients of other important precautionary information. 100 104 (See Cautions.) Preparations Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details. Please refer to the ASHP Drug Shortages Resource Center for information on shortages of one or more of these preparations. * available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name Bacitracin Routes Dosage Forms Strengths Brand Names Manufacturer Parenteral For injection, for IM use 50,000 units* BACiiM X-Gen Bacitracin for Injection AHFS DI Essentials. Copyright 2017, Selected Revisions May 4, 2016. American Society of Health-System Pharmacists, Inc., 4500 East-West Highway, Suite 900, Bethesda, Maryland 20814. † Use is not currently included in the labeling approved by the US Food and Drug Administration. References 7. Bacitracin. In: U.S. pharmacopeia, 38th rev, and The national formulary, 33rd ed. Rockville, MD: The United States Pharmacopeial Convention. From UPS-NF online. Accessed 2015 Nov 12. 14. Bacitracin. In: Martindale: The complete drug reference. London: Pharmaceutical Press; 2015. From MedicinesComplete website. Accessed 2015 Nov 11. 100. X-gen Pharmaceuticals, Inc. BACiiM (bacitracin) lyophilized powder for injection for IM use prescribing information. Big Flatts, NY. 2012 Jun. 101. Chang TW, Gorbach SL, Bartlett JG et al. Bacitracin treatment of antibiotic-associated colitis and diarrhea caused by Clostridium difficile toxin. Gastroenterology . 1980; 78:1584-6. [PubMed 7372074] 102. Young GP, Ward PB, Bayley N et al. Antibiotic-associated colitis due to Clostridium difficile : double-blind comparison of vancomycin with bacitracin. Gastroenterology . 1985; 89:1038-45. [PubMed 4043661] 103. Dudley MN, McLaughlin JC, Carrington G et al. Oral bacitracin vs vancomycin therapy for Clostridium difficile -induced diarrhea: a randomized double-blind trial. Arch Intern Med . 1986; 146:1101-4. [PubMed 3521518] 104. Pharmacia & Upjohn Company division of Pfizer. Bacitracin lyophilized powder for injection, USP, for IM use prescribing information. New York, NY. 2013 Oct. 106. Bond GC, Himelick RE, Macdonald LH. The stability of bacitracin. J Am Pharm Assoc . 1949; 38:30-4. 110. Cohen SH, Gerding DN, Johnson S et al. Clinical practice guidelines for Clostridium difficile infection in adults: 2010 update by the Society for Healthcare Epidemiology of America (SHEA) and the Infectious Diseases Society of America (IDSA). Infect Control Hosp Epidemiol . 2010; 31:431-55. [PubMed 20307191] 111. Fekety R for the American College of Gastroenterology Practice Parameters Committee. Guidelines for the diagnosis and management of Clostridium difficile - associated diarrhea and colitis. Am J Gastroenterol . 1997; 92:739-50. [PubMed 9149180] 112. American Society of Health-System Pharmacists Commission on Therapeutics. ASHP therapeutic position statement on the preferential use of metronidazole for the treatment of Clostridium difficile -associated disease. Am J Health-Syst Pharm . 1998; 55:1407-11. [PubMed 9659970] 113. Venugopal AA, Johnson S. Current state of Clostridium difficile treatment options. Clin Infect Dis . 2012; 55 Suppl 2:S71-6. 114. Food and Drug Administration. List of orphan designations and approvals. From FDA website. Accessed 2015 Nov 2. 115. Souney PF, Braun L, Steele L et al. Stability of bacitracin solution frozen in glass vials or plastic syringes. Am J Hosp Pharm . 1987; 44:1125-6. [PubMed 3605124] 117. Kelly CP, Pothoulakis C, LaMont JT. Clostridium difficile colitis. N Engl J Med . 1994; 330:257-62. [PubMed 8043060] 137. Bradley JS, Byington CL, Shah SS et al. The management of community-acquired pneumonia in infants and children older than 3 months of age: clinical practice guidelines by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America. Clin Infect Dis . 2011; 53:e25-76. 138. Mandell LA, Wunderink RG, Anzueto A et al. Infectious Diseases Society of America/American Thoracic Society consensus guidelines on the management of community-acquired pneumonia in adults. Clin Infect Dis . 2007; 44 Suppl 2:S27-72. [PubMed 17278083] 139. Anon. Choice of antibacterial drugs. Med Lett Treat Guid . 2007; 5:33-50. 140. Nelson R. Antibiotic treatment for Clostridium difficile-associated diarrhea in adults. Cochrane Database Syst Rev . 2007; :CD004610. 141. Bourgault AM, Lamothe F, Loo VG et al. In vitro susceptibility of Clostridium difficile clinical isolates from a multi-institutional outbreak in Southern Québec, Canada. Antimicrob Agents Chemother . 2006; 50:3473-5. [PubMed 17005836] 142. Bacon AE, McGrath S, Fekety R et al. In vitro synergy studies with Clostridium difficile. Antimicrob Agents Chemother . 1991; 35:582-3. [PubMed 2039211] 143. McMaster-Baxter NL, Musher DM. Clostridium difficile: recent epidemiologic findings and advances in therapy. Pharmacotherapy . 2007; 27:1029-39. [PubMed 17594209] 144. Kucers A, Crowe S, Grayson ML et al, eds. The use of antibiotics. A clinical review of antibacterial, antifungal, and antiviral drugs. 5th ed. Jordan Hill, Oxford: Butterworth-Heinemann; 1997: 542-3. 145. Briggs GG, Freeman RK, Yaffe SJ. Drugs in pregnancy and lactation. 8th ed. Baltimore, MD: Williams & Wilkins; 2008:162-3. a. AHFS drug information 2016. McEvoy GK, ed. Bacitracin. Bethesda, MD: American Society of Health-System Pharmacists; 2016. Next Interactions Print this page Add to My Med List More about BACiiM (bacitracin) Side Effects Breastfeeding Dosage Information Drug Interactions Support Group En Español 0 Reviews Add your own review/rating Drug class: miscellaneous antibiotics Consumer resources Baci-IM injection BACiiM Professional resources BACiiM (FDA) Bacitracin (AHFS Monograph) Related treatment guides Pneumonia> ]} 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 C Pregnancy Category Risk cannot be ruled out N/A CSA Schedule Not a controlled drug Approval History Drug history at FDA Drug Class Miscellaneous antibiotics Related Drugs Pneumonia ciprofloxacin , amoxicillin , azithromycin , doxycycline , metronidazole , Augmentin , Zithromax , Levaquin , levofloxacin , clindamycin , Bactrim , sulfamethoxazole / trimethoprim , cefdinir , ceftriaxone , Flagyl , vancomycin , cefuroxime , erythromycin , Rocephin , Ceftin , gentamicin , clarithromycin , amoxicillin / clavulanate , More... 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occasion [0.0001:<0.01 Mechanical ventilation 2.4 0.7 p> <0.05 Tube-feeding 10.0 3.6 p> <0.01 Length of hospital stay was also analyzed by patient age in both the adequate and well-controlled study and in an open label study. Age (days) Mean Length of Hospital Stay in Weeks Placebo * N=63 BabyBIG (RCT) N=59 BabyBIG (OLS) N=206 RCT = randomized clinical trial OLS = open label study * Both Gammagard 5% and Gammagard S/D 5% were used as placebo in this study. 0-60 3.8 (N=10) 2.8 (N=10) 2.0 (N=46) 61-120 5.6 (N=29) 1.9 (N=17) 2.0 (N=68) >120 6.6 (N=24) 3.0 (N=32) 1.8 (N=92) The observed reduction in length of hospital stay was statistically significant (p> <0.01) with the exception of the 0 to 60-day age stratum, where small patient numbers limited the statistical power. Length of hospital stay was analyzed in the adequate and well-controlled study by race (white versus non-white): RACE Mean Length of Hospital Stay in Weeks Placebo * BabyBIG (RCT) * Both Gammagard 5% and Gammagard S/D 5 % were used as placebo in this study. White 6.3 (N=40) 2.8 (N=35) Non-white 4.6 (N=23) 2.4 (N=24) Length of hospital stay was significantly reduced in both white and non-white patients (p=0.002). BabyBIG has not been tested for safety and efficacy in adults. REFERENCES Cytogam , cytomegalovirus immune globulin intravenous (human) (CMV-IGIV). In: Physician's Desk Reference. 55th Ed. Montvale, New Jersey: Medical Economics Company, Inc.; 2001:1861-1863. Immune globulin intravenous (human) Iveegam En IGIV. In: Physician's Desk Reference. 55th Ed. Montvale, New Jersey: Medical Economics Company, Inc.; 2001:816-820. Immune globulin intravenous (human) (IGIV) Gammagard S/D. In: Physician's Desk Reference. 55th Ed. Montvale, New Jersey: Medical Economics Company, Inc.; 2001:812-815. Immune globulin intravenous (human) Sandoglobulin lyophilized preparation. In: Physician's Desk Reference. 55th Ed. Montvale, New Jersey: Medical Economics Company, Inc.; 2001:2210-2213. Perazella MA, Cayco AV. Acute renal failure and intravenous immune globulin: sucrose nephropathy in disguise? Am J Ther 1998; 5:399-403. Cayco AV, Perazella MA, Hayslett JP. Renal insufficiency after intravenous immune globulin therapy: a report of two cases and an analysis of the literature. J Am Soc Nephrol 1997; 8:1788-1793. Important Drug Warning ("Dear Doctor") letter. Center for Biologics Evaluation and Research, Food and Drug Administration, 1998. Denepoux S, et al. Molecular characterization of human IgG monoclonal antibodies specific for major birch pollen allergen Bet v 1. Anti-allergen IgG can enhance the anaphylactic reaction. FEBS Lett 2000; 465:39-46. Burks AW, Sampson HA, Buckley RH. Anaphylactic reactions after gamma globulin administration in patients with hypogammaglobulinemia. Detection of IgE antibodies to IgA. N Engl J Med 1986; 314:560-564. Sekul EA, Cupler EJ, Dalakas MC. Aseptic meningitis associated with high-dose intravenous immunoglobulin therapy: frequency and risk factors. Ann Intern Med 1994; 121:259-262. Kato E, Shindo S, Eto Y, et al. Administration of immune globulin associated with aseptic meningitis. JAMA 1988; 259:3269-3270. Casteels-Van Daele M, Wijndaele L, Hunninck K. Intravenous immunoglobulin and acute aseptic meningitis. N Engl J Med 1990; 323:614-615. Scribner C, Kapit R, Philips E, Rickels N. Aseptic meningitis and intravenous immunoglobulin therapy. Ann Intern Med 1994; 121:305-306. Arnon SS, Schechter R, Maslanka SE, Jewell NP, Hatheway CL. Human botulism immune globulin for the treatment of infant botulism. N Engl J Med 2006; 354:462-471. Arnon SS. Creation and development of the public service orphan drug Human Botulism Immune Globulin. Pediatrics 2007; 119:785-789. Long SS, Gajewski JL, Brown LW, Gilligan PH. Clinical, laboratory, and environmental features of infant botulism in southeastern Pennsylvania. Pediatrics 1985; 75:935-941. Schreiner MS, et al. Infant botulism: a review of 12 years' experience at the Children's Hospital of Philadelphia. Pediatrics 1991; 87:159-165. Wilson R, et al. Clinical characteristics of infant botulism in the United States: a study of the non-California cases. Pediatr Infect Dis 1982; 1:148-150. Anderson TD, et al. Airway complications of infant botulism: ten-year experience with 60 cases. Otolaryngol Head Neck Surg 2002; 126:234-239. Arnon SS. Infant botulism. In: Textbook of Pediatric Infectious Diseases. 5th ed. Philadelphia: WB Saunders 2004; 1758-1766. Snydman DR, Werner BG, Tilney NL, et al. Final analysis of primary cytomegalovirus disease prevention in renal transplant recipients with cytomegalovirus immune globulin: comparison of the randomized and open-label trials. Transplant Proc 1991; 23:1357-1360. Tseng-Ong L, Mitchell WG. Infant botulism: 20 years' experience at a single institution. J Child Neurol 2007; 22:1333-1337. Underwood K, Rubin S, Deakers T, Newth C. Infant botulism: A 30-year experience spanning the introduction of botulism immune globulin intravenous in the intensive care unit at Childrens Hospital Los Angeles. Pediatrics 2007; 120:e1380-e1385. Siber GR, Syndman DR. Use of immune globulins in the prevention and treatment of infections. Curr Clin Top Infect Dis 1992; 12:208-256. Berkman SA, Lee ML, Gale RP. Clinical uses of intravenous immunoglobins. Ann Intern Med 1990; 112:278-292. Bossell J, et al. Safety of therapeutic immune globulin preparations with respect to transmission of human T-lymphotropic virus type III/lymphadenopathy-associated virus infection. Morb Mortal Wkly Rep 1986; 35:231-233. Wells MA, Wittek AE, Epstein JS, et al. Inactivation and partition of human T-cell lymphotrophic virus, type III, during ethanol fractionation of plasma. Trans 1986; 26:210-213. Horowitz B, Wiebe ME, Lippin A, Stryker MH. Inactivation of viruses in labile blood derivatives. I. Disruption of lipid-enveloped viruses by tri(n-butyl)phosphate detergent combinations. Transfusion 1985; 25:516-522. Edwards CA, Piet MPJ, Chin S, Horowitz B. Tri(n-butyl) phosphate/detergent treatment of licensed therapeutic and experimental blood derivatives. Vox Sang 1987; 52:53-59. Paton JC, Lawrence AL, Steven IM. Quantitation of Clostridium botulinum organisms and toxin in feces and presence of Clostridium botulinum toxin in the serum of an infant with botulism. J Clin Microbiol 1983; 17:13-15. Rizk A, Gorson KC, Kenney L, Weinstein R. Transfusion-related acute lung injury after the infusion of IVIG. Transfusion 2001; 41: 264-268. How Supplied/Storage and Handling NDC 68403-1100-6, 100 mg 20 mg lyophilized immunoglobulin single-dose vial individually packaged in a carton, supplied with 2 mL Sterile Water for Injection USP for reconstitution. Store the vial containing the lyophilized product between 2° and 8°C (35.6° to 46.4°F). Do not store BabyBIG in the reconstituted state. Use reconstituted BabyBIG within 2 hours. Do not use beyond expiration date, and dispose unused product in accordance with local requirements. Patient Counseling Information Discuss the risks and benefits of BabyBIG use with the patient's legal guardians, including the possibility of adverse reactions, e.g., hypersensitivity reactions such as anaphylaxis, as well as aseptic meningitis, TRALI, hemolysis, renal failure, and thrombosis [ see WARNINGS AND PRECAUTIONS (5) ]. Inform patient's legal guardians that BabyBIG is made from human plasma and may contain infectious agents that can cause disease. While the risk of transmitting an infection has been reduced by screening plasma donors for prior exposure, testing donated plasma, and inactivating or removing certain viruses during manufacturing, the patient's guardian should report any symptoms that concern them [see WARNINGS AND PRECAUTIONS (5.3) ]. Inform patient's legal guardians that BabyBIG may interfere with immune response to live viral vaccines (e.g., MMR) and instruct them to notify the healthcare provider of this potential interaction when the patient is to receive vaccinations [ see DRUG INTERACTIONS (7) ]. For additional information concerning BabyBIG, contact: Infant Botulism Treatment and Prevention Program California Department of Public Health 850 Marina Bay Parkway, Room E-361 Richmond, California 94804 Telephone: 510-231-7600 US Govt. License No. 1797 Manufactured by: Baxter Healthcare Corporation Westlake Village, CA 91362, USA US Govt. License No. 140; and Cangene Corporation Winnipeg, Manitoba, R3T 5Y3, Canada US Govt. License No. 1201 Distributed by: FFF Enterprises Temecula, California 92591, USA Distributed for: Infant Botulism Treatment and Prevention Program California Department of Public Health 850 Marina Bay Parkway, Room E-361 Richmond, California 94804 Revised October 2011 PRINCIPAL DISPLAY PANEL - 2 mL Vial Label Botulism Immune Globulin Intravenous (Human) (BIG-IV) BabyBIG DO NOT SHAKE VIAL AFTER RECONSTITUTION; AVOID FOAMING. See package insert for reconstitution, dosage, and administration. Rx only. Single use container. Manufactured for: California Department of Public Health by: Baxter Healthcare Corporation and Cangene Corporation LOT EXP. PRINCIPAL DISPLAY PANEL - 1 Single Use Vial Carton NDC 68403-1100-6 Rx Only 100 mg IgG, 100 mg Sucrose 20 mg Albumin (Human) Lyophilized Solvent Detergent Treated Botulism Immune Globulin Intravenous (Human) (BIG-IV) BabyBIG Store between 2°C and 8°C (35.6°F and 46.4°F). BabyBIG human botulinum neurotoxin a/b immune globulin injection, powder, lyophilized, for solution Product Information Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:68403-1100 Route of Administration INTRAVENOUS DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength human botulinum neurotoxin a/b immune globulin (human botulinum neurotoxin a/b immune globulin) human botulinum neurotoxin a/b immune globulin 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength sucrose 50 mg in 1 mL albumin human 10 mg in 1 mL sodium phosphate, monobasic, anhydrous Packaging # Item Code Package Description 1 NDC:68403-1100-6 1 VIAL, SINGLE-USE in 1 CARTON 1 2 mL in 1 VIAL, SINGLE-USE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA125034 10/23/2003 Labeler - CALIFORNIA DEPARTMENT OF PUBLIC HEALTH (004519216) Establishment Name Address ID/FEI Operations Baxalta Inc. 085206634 MANUFACTURE(68403-1100) Establishment Name Address ID/FEI Operations Cangene BioPharma Inc. 050783398 MANUFACTURE(68403-1100) Establishment Name Address ID/FEI Operations Catalent Pharma Solutions 962674474 LABEL(68403-1100), PACK(68403-1100) Revised: 11/2015 CALIFORNIA DEPARTMENT OF PUBLIC HEALTH Next Interactions Print this page Add to My Med List More about BabyBIG (botulism immune globulin) Side Effects Dosage Information Drug Interactions Support Group En Español 0 Reviews Add your own review/rating Drug class: immune globulins Consumer resources BabyBIG Professional resources BabyBIG (AHFS Monograph) Related treatment guides Botulism> ]} 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 Drug Class Immune globulins Related Drugs immune globulins Gammagard , RhoGAM , Hizentra , Synagis , Privigen , Gamunex Botulism penicillin g sodium , Pfizerpen , botulism antitoxin , More... 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if you want to Baciguent Generic Name: bacitracin topical (BAS i TRAY sin TOP i kal) Brand Name: Baciguent Overview Side Effects Professional Breastfeeding Reviews More Support Group Q & A What is bacitracin? Bacitracin is an antibiotic that fights bacteria. Bacitracin topical (for the skin) is used to prevent infection in minor cuts, scrapes, and burns. Bacitracin may also be used for purposes not listed in this medication guide. Slideshow Amoxicillin: 13 Burning Questions What is the most important information I should know about bacitracin? Follow all directions on your medicine label and package. Tell each of your healthcare providers about all your medical conditions, allergies, and all medicines you use. What should I discuss with my health care provider before using bacitracin? You should not use this medicine if you are allergic to bacitracin, mineral oil, or petroleum jelly. Do not use bacitracin topical to treat animal bites, puncture wounds, deep skin wounds, or severe burns. Ask a doctor or pharmacist if it is safe for you to use this medicine if you are not sure. Bacitracin is not expected to harm an unborn baby. It is not known whether bacitracin passes into breast milk or if it could harm a nursing baby. Ask a doctor or pharmacist if it is safe for you to use this medicine if you are pregnant or breast-feeding. How should I use bacitracin? 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. Clean the skin area before applying bacitracin topical. You may apply bacitracin to the affected area 1 to 3 times per day. Apply only enough to cover the area you are treating. Do not use this medication over large areas of skin. You may cover the treated skin with a bandage. Do not use bacitracin for longer than 7 days in a row. Call your doctor if your symptoms do not improve after 7 days of treatment, or if you develop a skin rash. Store at room temperature away from moisture and heat. Do not freeze. What happens if I miss a dose? Since bacitracin topical is when needed, you are not likely to miss a 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 using bacitracin? Bacitracin topical is for use only on the skin. Avoid getting this medication in your eyes, nose, mouth, rectum, or vagina. If this does happen, rinse with water. Bacitracin side effects Get emergency medical help if you have signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat. Less serious side effects are more likely, and you may have none at all. 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 bacitracin? It is not likely that other drugs you take orally or inject will have an effect on topically applied bacitracin. 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 Baciguent (bacitracin topical) Side Effects Breastfeeding Support Group En Español 0 Reviews Add your own review/rating Drug class: topical antibiotics Professional resources Baciguent topical (AHFS Monograph) Related treatment guides Bacterial Skin Infection Where can I get more information? Your pharmacist can provide more information about bacitracin 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: 3.01. Date modified: December 03, 2017 Last reviewed: September 30, 2015 Drug Status Rx OTC Availability Rx and/or OTC N Pregnancy Category Not classified N/A CSA Schedule Not a controlled drug Drug Class Topical antibiotics Related Drugs Bacterial Skin Infection Bactrim , sulfamethoxazole / trimethoprim , Bactrim DS , bacitracin topical , tetracycline topical , Septra , Neosporin , SMZ-TMP DS , Septra DS , Triple Antibiotic , Co-trimoxazole , Sulfatrim , Polysporin First Aid Antibiotic Ointment , Cortisporin Cream , Cotrim , Antibiotic Plus Pain Relief , Sulfatrim Pediatric , Cortisporin Ointment , Neo-Synalar , More... Baciguent 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 Baciguent support group to connect with others who have similar interests. a chronic


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Photo :BabyBIG
divulge to BabyBIG Generic Name: botulism immune globulin (BOT ue lizm im MYOON GLOB yoo lin) Brand Name: BabyBIG Overview Side Effects Dosage Professional Interactions More User Reviews Support Group Q & A What is BabyBIG (botulism immune globulin)? Botulism immune globulin is a sterilized solution made from human plasma. It contains the antibodies to help your body protect itself against infection caused by botulism toxin type A and B. Botulism immune globulin is used to treat infant botulism caused by toxin type A or B. This medicine is used in children who are younger than 1 year old. Botulism immune globulin may also be used for purposes not listed in this medication guide. Slideshow Understanding Insulin: What You Need To Know What is the most important information I should know about BabyBIG (botulism immune globulin)? Your baby should not receive this medicine if he or she has immune globulin A (IgA) deficiency with antibody to IgA. Your baby should not receive a "live" vaccine (measles, mumps, rubella, polio, rotavirus, yellow fever, varicella) for at least 3 months after receiving botulism immune globulin. What should I discuss with my healthcare provider before my child receives BabyBIG (botulism immune globulin)? Your baby should not receive botulism immune globulin if he or she has ever had an allergic reaction to an immune globulin, or if the child has immune globulin A (IgA) deficiency with antibody to IgA. To make sure botulism immune globulin is safe for your baby, tell the doctor if your baby has: kidney disease; diabetes; if the baby has recently received any vaccination; if the baby is dehydrated; or if the baby is being treated with any medicines that weaken the immune system. Botulism immune globulin is made from human plasma (part of the blood) which may contain viruses and other infectious agents. Donated plasma is tested and treated to reduce the risk of it containing infectious agents, but there is still a small possibility it could transmit disease. Talk with your doctor about the risks and benefits of using this medication. How is BabyBIG (botulism immune globulin)given? To best participate in the care of your baby while he or she is being treated with botulism immune globulin, carefully follow all instructions provided by your baby's caregivers. Botulism immune globulin is injected into a vein through an IV. Your baby will receive this IV infusion in a clinic or hospital setting. Botulism immune globulin is usually given as a one-time treatment. Your baby's breathing, blood pressure, oxygen levels, and other vital signs will be watched closely during the infusion. To be sure botulism immune globulin is not causing harmful effects, your baby may need follow-up blood tests. What happens if a dose is missed? Since botulism immune globulin is used as a single dose, it does not have a daily dosing schedule. What happens if an overdose is given? Since this medicine is given by a healthcare professional in a medical setting, an overdose is unlikely to occur. What should be avoided after receiving BabyBIG (botulism immune globulin)? Your baby should not receive a "live" vaccine for at least 3 months after receiving botulism immune globulin. Live vaccines include measles, mumps, rubella, polio, rotavirus, yellow fever, and varicella. The vaccine may not work as well during this time, and may not fully protect your baby from disease. BabyBIG (botulism immune globulin) side effects Your baby will remain under constant supervision during treatment with botulism immune globulin. Get emergency medical help if your baby has 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 the baby has: tenderness, redness, warmth, cold feeling, or blue/purple appearance in the arms or legs; fussiness, trouble breathing, blue lips, pale skin; little or no urinating, fewer wet diapers than usual; yellowed skin, dark colored urine; low levels of sodium in the body--confusion, severe weakness, vomiting, loss of coordination or motor skills; or swelling around the brain or spinal cord--fever, neck stiffness, sensitivity to light, weakness, sleepiness, vomiting. Common side effects may include: mild skin rash or redness on the baby's face, chest, back, or stomach; chills, body aches; wheezing; or 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 BabyBIG (botulism immune globulin)? Other drugs may interact with botulism immune globulin, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell your baby's doctor about all medicines your baby receives. Next Side Effects Print this page Add to My Med List More about BabyBIG (botulism immune globulin) Side Effects Dosage Information Drug Interactions Support Group En Español 0 Reviews Add your own review/rating Drug class: immune globulins Professional resources BabyBIG (AHFS Monograph) BabyBIG (FDA) Related treatment guides Botulism Where can I get more information? Your doctor or pharmacist can provide more information about botulism immune globulin. 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: 2.01. Date modified: December 03, 2017 Last reviewed: March 06, 2014 Drug Status Rx Availability Prescription only N Pregnancy Category Not classified N/A CSA Schedule Not a controlled drug Drug Class Immune globulins Related Drugs Botulism penicillin g sodium , Pfizerpen , botulism antitoxin , More... BabyBIG 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 BabyBIG support group to connect with others who have similar interests. left out


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Photo :Baby Orajel Liquid
benefit from Baby Orajel Liquid Generic Name: benzocaine (Oral route, Oromucosal route) BEN-zoe-kane 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. Anbesol Babee Teething Benzodent Benz-O-Sthetic Bi-Zets/Benzo-Troches Dentemp's Dent-O-Kain/20 Detane Gumsol HAD Hurricaine Hurricane Spray Kit Kank-A Soft Brush Larynex Miradyne-3 Mycinette Orabase-B Oracaine Ora film Orajel OraMagic Plus Orasol Red Cross Canker Sore Thorets Trocaine Zetts Zilactin Zilactin-B In Canada Anbesol Extra Strength Anbesol Liquid Baby Anbesol Baby Orajel Baby Orajel Liquid Maximum Strength Orajel Pm Orajel Extra Strength Available Dosage Forms: Gel/Jelly Liquid Solution Film Lozenge/Troche Lotion Ointment Powder for Suspension Cream Tablet, Disintegrating Swab Spray Gum Paste Therapeutic Class: Anesthetic, Local Chemical Class: Amino Ester Slideshow All Eyes On Ibuprofen: What You Need To Know Uses For Baby Orajel Liquid Benzocaine lozenges are used to relieve pain and irritation caused by sore throat, sore mouth, or canker sores. This medicine is available without a prescription; however, your doctor may have special instructions on the proper use and dose for your medical problem. Before Using Baby Orajel Liquid 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 No information is available on the relationship of age to the effects of benzocaine lozenges in the pediatric population. Safety and efficacy have not been established in children below 5 years of age. Geriatric No information is available on the relationship of age to the effects of benzocaine in geriatric patients. 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. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco. 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: Infection in or around your mouth or Large sores in or around your mouth The chance of side effects may be increased. Proper Use of benzocaine This section provides information on the proper use of a number of products that contain benzocaine. It may not be specific to Baby Orajel Liquid. Please read with care. Use this medicine exactly as directed by your doctor . Do not use more of this medicine, do not use it more often, and do not use it for a longer time than directed. To do so may increase the chance of absorption into the body and the risk of side effects. This medicine should be used only for problems being treated by your doctor or conditions listed in the package directions. Check with your doctor before using it for other problems, especially if you think that an infection may be present . Do not use this medicine for more than 2 days without checking first 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 (lozenges): For sore throat and mouth pain: Adults, teenagers, and children 5 years of age and older One lozenge, dissolved slowly in the mouth every 2 hours as needed. Children younger than 5 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. Ask your healthcare professional how you should dispose of any medicine you do not use. Precautions While Using Baby Orajel Liquid If your condition does not improve within 7 days, or if it becomes worse, check with your doctor. Call your doctor right away if you start to have a severe sore throat or sore throat that occurs with a high fever, headache, nausea, or vomiting. These maybe signs of an infection. Baby Orajel Liquid 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: Incidence not known Headache high fever nausea vomiting worsening of pain, redness, swelling, or irritation in or around the mouth 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 Orajel Baby (benzocaine topical) Side Effects During Pregnancy or Breastfeeding Dosage Information Drug Interactions Support Group 0 Reviews Add your own review/rating Drug class: topical anesthetics Consumer resources Baby Orajel (Advanced Reading) Baby Orajel Nighttime Formula (Advanced Reading) Other brands: Orabase , Anbesol , Dermoplast , Lanacane , ... +26 more Professional resources Baby Orajel Teething Medicine (FDA) Benzocaine topical (AHFS Monograph) Other Formulations Orajel Related treatment guides Oral and Dental Conditions} 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 Oral and Dental Conditions benzocaine topical , Orajel , hydrogen peroxide topical , Orabase , Anbesol , Hurricaine , Topex , Cepacol Ultra , Benzo-Jel , Trocaine , Zilactin-B , OraMagic Plus , Dent-O-Kain , Kank-a , More... Orajel Baby 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 Orajel Baby support group to connect with others who have similar interests.} } can probably


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Photo :Baby Orajel Nighttime Formula (Topical application)
possibly Baby Orajel Nighttime Formula (Topical application) Generic Name: benzocaine (Topical application route) BEN-zoe-kane 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. Anacaine Chiggerex Mandelay Medicone Outgro Solarcaine In Canada Baby Orajel Nighttime Formula Dermoplast Maximum Strength Topicaine Available Dosage Forms: Ointment Spray Liquid Gel/Jelly Cream Wax Solution Therapeutic Class: Anesthetic, Local Chemical Class: Amino Ester Slideshow All Eyes On Ibuprofen: What You Need To Know Uses For Baby Orajel Nighttime Formula Benzocaine is used to relieve pain and itching caused by conditions such as sunburn or other minor burns, insect bites or stings, poison ivy, poison oak, poison sumac, minor cuts, or scratches. Benzocaine belongs to a group of medicines known as topical local anesthetics. It deadens the nerve endings in the skin. This medicine does not cause unconsciousness like general anesthetics do when used for surgery. This medicine is available without a prescription; however, your doctor may have special instructions on the proper use and dose for your medical condition. Before Using Baby Orajel Nighttime Formula 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 Because of benzocaine's toxicity, use in children under 2 years of age is not recommended. Geriatric No information is available on the relationship of age to the effects of benzocaine in geriatric patients. 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. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco. 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 Glucose-6-phosphodiesterase deficiency (a hereditary metabolic disorder affecting red blood cells) or Hemoglobin-M disease (a hereditary metabolic disorder affecting red blood cells) or NADH-methemoglobin reductase deficiency (a hereditary metabolic disorder affecting red blood cells) or Pyruvate-kinase deficiency (a hereditary metabolic disorder affecting red blood cells) Use with caution. May increase the risk of developing a serious side effect called methemoglobinemia. Asthma or Bronchitis or Emphysema or Heart disease or Infection at the place of application or Large sore, broken skin, or injury at the place of application or Smokers Use with caution. May cause side effects to become worse. Children under the age of 2 years Should not be used in this age group. Proper Use of benzocaine This section provides information on the proper use of a number of products that contain benzocaine. It may not be specific to Baby Orajel Nighttime Formula. Please read with care. Use this medicine exactly as directed by your doctor . Do not use it for any other reason without first checking with your doctor. This medicine may be more likely than other topical anesthetics to cause unwanted effects if it is used too much, because more of it is absorbed into the body through the skin. Wash your hands with soap and water before and after using this medicine. Unless otherwise directed by your doctor, do not apply this medicine to open wounds, burns, or broken or inflamed skin. This medicine should be used only for problems being treated by your doctor or conditions listed in the package directions. Check with your doctor before using it for other problems, especially if you think that an infection may be present . This medicine should not be used to treat certain kinds of skin infections or serious problems, such as severe burns. Be careful not to get any of this medicine in your nose, mouth, and especially in your eyes, because it can cause severe eye irritation. If any of the medicine does get into these areas especially the eyes, wash it with water for at least 15 minutes and check with your doctor right away. If you are using a spray form of this medicine, do not spray it directly on your face. Instead, use your hand or an applicator (e.g., a sterile gauze pad or a cotton swab) to apply the medicine. To use the pad or swab , open the package according to the directions. When treating a bee sting, remove the stinger before using the medicine. Wipe the pad or swab across the affected skin area. Read the package label very carefully to see if the product contains any alcohol. Alcohol is flammable and can catch on fire. Do not use any product containing alcohol near a fire or open flame, or while smoking. Also, do not smoke after applying one of these products until it has completely dried . If you are using the gel or liquid form: Use the benzocaine gel or liquid only when needed, but not for more than four times a day. In children, instead of using this medicine, talk with your pediatrician about different ways to treat teething. Give your child a chilled teething ring, or gently rub or massage your child's gums with your finger to relieve symptoms of teething pain. Do not use this medicine in children under the age of 2 unless your doctor tells you to. 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 topical dosage forms (aerosol spray, pads, or swabs): For pain and itching caused by minor skin conditions: Adults, teenagers, and children 2 years of age and older Apply to the affected area three or four times a day as needed. Children younger than 2 years of age Use and dose must be determined by your doctor. Missed Dose If you miss a dose of this medicine, apply 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. Storage Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing. Store the canister at room temperature, away from heat and direct light. Do not freeze. Do not keep this medicine inside a car where it could be exposed to extreme heat or cold. Do not poke holes in the canister or throw it into a fire, even if the canister is empty. Keep out of the reach of children. Do not keep outdated medicine or medicine no longer needed. Ask your healthcare professional how you should dispose of any medicine you do not use. Precautions While Using Baby Orajel Nighttime Formula If your or your child's condition does not improve within 7 days, or if it becomes worse, check with your doctor. After applying this medicine to the skin of your child, watch the child carefully to make sure that he or she does not get any of the medicine into his or her eyes or mouth . It can cause serious side effects, especially in children, if any of the medicine gets into the mouth or is swallowed. Stop using this medicine and check with your doctor right away if you or your child have a skin rash, burning, stinging, swelling, or irritation of your skin. Do not use cosmetics or other skin care products on the treated skin areas. This medicine may cause a rare, but serious blood problem called methemoglobinemia. This condition may occur after use of the spray for medical procedures or use of the over-the-counter gel or liquid for mouth sores or teething in children. The risk may be increased in infants younger than 4 months of age, elderly patients, or patients with certain inborn defects. It has occurred when patients receive too much of the medicine, but can also occur with small amounts. Make sure you store this medicine out of reach of children. Call your doctor right away if you or your child has the following symptoms after receiving this medicine: pale, gray, or blue-colored skin, lips, or nails; confusion; headache; lightheadedness; fast heartbeat; shortness of breath; or unusual tiredness or weakness. Make sure your doctor knows if you are also taking medicines containing nitrates or nitrites. This includes nitroglycerin, Imdur , Isordil , Nitro-Bid , Nitrostat , or Transderm-Nitro . Baby Orajel Nighttime Formula 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: Rare Bluish color of the fingernails, lips, skin, palms, or nail beds Incidence not known Blistering, burning, crusting, dryness, or flaking of the skin cracking, itching, redness, or stinging of the skin dark urine difficulty with breathing difficulty with walking dizziness or lightheadedness fainting fever headache inability to feel hands and feet irritability irritation of the nose itching, scaling, severe redness, soreness, or swelling of the skin pale skin rapid heart rate red, sore eyes shortness of breath sore throat unusual bleeding or bruising unusual drowsiness, dullness, tiredness, weakness, or feeling of sluggishness 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 Orajel Baby (benzocaine topical) Side Effects During Pregnancy or Breastfeeding Dosage Information Drug Interactions Support Group 0 Reviews Add your own review/rating Drug class: topical anesthetics Consumer resources Baby Orajel (Advanced Reading) Baby Orajel Liquid (Advanced Reading) Other brands: Orabase , Anbesol , Dermoplast , Lanacane , ... +26 more Professional resources Baby Orajel Teething Medicine (FDA) Benzocaine topical (AHFS Monograph) Other Formulations Orajel Related treatment guides Oral and Dental Conditions} 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 Oral and Dental Conditions benzocaine topical , Orajel , hydrogen peroxide topical , Orabase , Anbesol , Hurricaine , Topex , Cepacol Ultra , Trocaine , Benzo-Jel , Zilactin-B , OraMagic Plus , Kank-a , Dent-O-Kain , More... Orajel Baby 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 Orajel Baby support group to connect with others who have similar interests.} } good deal


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