Lidokain SAD may be available in the countries listed below.
Lidocaine hydrochloride (a derivative of Lidocaine) is reported as an ingredient of Lidokain SAD in the following countries:
International Drug Name Search
Estrogens have been reported to increase the chance of womb (endometrial) cancer. Estrogen-containing products should not be used to prevent heart disease or dementia. Estrogen given alone or in combination with another hormone (progestin) for replacement therapy may increase your risk for heart disease (eg, heart attacks), stroke, serious blood clots in the legs (deep vein thrombosis) or lungs (pulmonary embolism), dementia, or breast cancer. These risks appear to depend on the length of time Climara Pro Weekly Patch is used and the amount of estrogen per dose. Therefore, Climara Pro Weekly Patch should be used for the shortest possible length of time at the lowest effective dose, so that you obtain the benefits and minimize the chance of serious side effects from long-term treatment. Consult your doctor or pharmacist for details.
Treating certain symptoms of menopause (eg, hot flashes). It is used to prevent osteoporosis (weak bones) after menopause in certain patients. It may also be used for other conditions as determined by your doctor.
Climara Pro Weekly Patch is an estrogen hormone used to provide the female hormone when the body no longer produces enough.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Climara Pro Weekly Patch. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Climara Pro Weekly Patch. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if Climara Pro Weekly Patch may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.
Use Climara Pro Weekly Patch as directed by your doctor. Check the label on the medicine for exact dosing instructions. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Climara Pro Weekly Patch.
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:
Headache; irregular vaginal bleeding or spotting; mild breast pain; mild hair loss; nausea; stomach cramps or bloating; vomiting.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); breast lumps; breast pain; calf pain or tenderness; changes in vision or speech (eg, change in contact lens fit, loss of vision); chest pain; coughing of blood; dizziness; fainting; mental or mood changes (eg, severe depression, memory loss); pain, swelling, or tenderness in the stomach; severe headache or vomiting; severe, persistent, or unusual vaginal bleeding; slurred speech; sudden shortness of breath; swelling of hands or feet; unusual vaginal discharge, itching, or odor; weakness or numbness of an arm or leg; yellowing of the skin or eyes.
This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.
See also: Climara Pro side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include excessive vaginal bleeding; severe nausea; vomiting.
Store Climara Pro Weekly Patch at room temperature, between 59 and 86 degrees F (15 and 30 degrees C), in the original sealed pouch. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Climara Pro Weekly Patch out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Climara Pro Weekly Patch. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.
Relieving sneezing, runny nose, and watery eyes due to colds, flu, or hay fever. It may also be used for other conditions as determined by your doctor.
RespiVent DF is an antihistamine and anticholinergic combination. It works by blocking a substance in the body that causes sneezing, runny nose, and watery eyes. It also dries the nose and chest.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with RespiVent DF. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with RespiVent DF. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if RespiVent DF may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.
Use RespiVent DF as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use RespiVent DF.
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:
Blurred vision; change in appetite; constipation; dizziness; drowsiness; dry mouth; fast heartbeat; nausea; nervousness; ringing in the ears; stomach upset or pain; sun sensitivity; trouble sleeping.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); confusion; difficulty urinating; fainting or feeling faint; fever; flushing; hallucinations; seizures; severe clumsiness; severe drowsiness; shortness of breath; sore throat; unusual bruising or bleeding; unusual tiredness or weakness.
This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.
See also: RespiVent DF side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include difficulty breathing; extreme dizziness; extreme drowsiness; fixed/large pupils; hot, dry skin; irregular heartbeat; loss of consciousness; mental or mood changes; persistent vomiting; ringing in the ears; seizures.
Store RespiVent DF at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep RespiVent DF out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about RespiVent DF. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.
Generic Name: belladonna, ergotamine, and phenobarbital (bel uh DON uh, er GOT uh meen, and feen oh BAR bit al)
Brand Names: Bel-Phen-Ergot, Bellamine, Bellamor, Bellaphen-S, Bellaspas, Bellergal-S, Duragal-S, Eperbel-S, Spastrin
Belladonna is a naturally occurring mixture that produces many effects in the body. It reduces spasms within the stomach and intestines, the bladder, and the biliary (liver) system. Belladonna also reduces the secretions of many organs, which helps control conditions such as excess stomach acid.
Ergotamine narrows the blood vessels involved in circulation to the head. Ergotamine can also alter blood flow patterns involved in vascular headaches, such as migraines.
Phenobarbital is a barbiturate that reduces brain and nervous system activity.
The combination of belladonna, ergotamine, and phenobarbital is used to treat symptoms of menopause including hot flashes, sweating, increased heart rate, dizziness, restlessness, headache, anxiety, and trouble sleeping.
Belladonna, ergotamine, and phenobarbital may also be used for purposes other than those listed in this medication guide.
Avoid using other medicines that make you sleepy (such as cold medicine, pain medication, muscle relaxers, and medicine for seizures, depression or anxiety). They can add to sleepiness caused by belladonna, ergotamine, and phenobarbital.
narrow-angle glaucoma;
heart disease;
liver disease;
kidney disease;
porphyria;
a history of circulation problems, stroke, or blood clots;
high blood pressure; or
if you are pregnant or breast-feeding.
Before using belladonna, ergotamine, and phenobarbital, tell your doctor if you have:
a stomach problem called pyloric obstruction; or
angina (chest pain).
If you have any of these conditions, you may not be able to use this medication, or you may need a dosage adjustment or special tests during treatment.
Take this medication exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor.
To be sure this medication is helping your condition, your doctor may need to check your progress on a regular basis. It is important that you not miss any scheduled visits to your doctor.
Take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at the next regularly scheduled time. Do not take extra medicine to make up the missed dose.
Avoid using other medicines that make you sleepy (such as cold medicine, pain medication, muscle relaxers, and medicine for seizures, depression or anxiety). They can add to sleepiness caused by belladonna, ergotamine, and phenobarbital.
Other less serious side effects are more likely to occur, such as:
blurred vision;
dry mouth;
warmth or tingly feeling;
drowsiness; or
changes in behavior (in children).
Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.
Before taking this medication, tell your doctor if you are using any of the following drugs:
a blood thinner such as warfarin (Coumadin);
birth control pills;
erythromycin (E-Mycin, Ery-Tab, Erythrocin, E.E.S.); or
troleandomycin (Tao).
If you are using any of these drugs, you may not be able to use belladonna, ergotamine, and phenobarbital, or you may need dosage adjustments or special tests during treatment.
There may be other drugs not listed that can affect belladonna, ergotamine, and phenobarbital. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.
Belladonna, ergotamine, and phenobarbital is available with a prescription under the brand names Bellergal, Bellamine, Bellaspas, Duragal-S, and Spastrin. Other brand or generic forms may also be available. Ask your pharmacist any questions you have about this medication, especially if it is new to you.
MembraneBlue is a brand name of trypan blue ophthalmic, approved by the FDA in the following formulation(s):
No. There is currently no therapeutically equivalent version of MembraneBlue available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of MembraneBlue. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: About generic drugs.
There are no current U.S. patents associated with MembraneBlue.
Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.
Generic Name: cholecalciferol, genistein, and zinc chelazome (KOE le kal SIF er ol, GEN i styne, and ZINK KEE la zome)
Brand names: Fosteum, Fosteum (obsolete)
Cholecalciferol is vitamin D3. Vitamin D is important for the absorption of calcium from the stomach and for the functioning of calcium in the body.
Genistein is an isoflavone derived from a plant source. Genistein reduces cells that break down bone and stimulates cells that build bone in the body. It also reverses the bone effects of estrogen loss in postmenopausal women. Genistein also works with zinc to promote bone mineralization, which hardens and strengthens bone tissue.
Zinc is a naturally occurring mineral. Zinc is important for growth and for the development and health of body tissues.
The combination of cholecalciferol, genistein, and zinc chelazome is a medical food product. It is used to slow the metabolic processes that cause bone loss and may lead to osteoporosis.
Cholecalciferol, genistein, and zinc chelazome may be used for other purposes not listed in this medication guide.
Before you take cholecalciferol, genistein, and zinc chelazome, tell your doctor if you have liver disease, a gallbladder disorder, a blood cell cancer such as leukemia or lymphoma, sarcoidosis (an autoimmune disorder), an electrolyte imbalance, or any condition that makes it hard for your body to absorb nutrients from food (malabsorption).
If you have certain conditions, you may need a dose adjustment or special tests to safely use this medication. Before you take cholecalciferol, genistein, and zinc chelazome, tell your doctor if you have:
liver disease;
a gallbladder disorder;
a blood cell cancer such as leukemia or lymphoma;
sarcoidosis (an autoimmune disorder);
an electrolyte imbalance; or
any condition that makes it hard for your body to absorb nutrients from food (malabsorption).
Use this medication exactly as prescribed by your doctor. Do not use it in larger amounts or for longer than recommended. Follow the directions on your prescription label.
Cholecalciferol, genistein, and zinc chelazome is usually taken twice daily, spaced 12 hours apart. Follow your doctor's instructions.
You may take cholecalciferol, genistein, and zinc chelazome with or without food. Take it with food if it upsets your stomach.
To be sure this medication is helping your condition, your blood and urine may need to be tested on a regular basis. Do not miss any scheduled appointments.
Cholecalciferol, genistein, and zinc chelazome is only part of a complete program of treatment that may also include diet, exercise, and calcium or other mineral supplementation. Follow your diet, medication, and exercise routines very closely.
Take the missed dose as soon as you remember. If it is almost time for your next dose, wait until then to take the medicine and skip the missed dose. Do not take extra medicine to make up the missed dose.
Overdose symptoms may include headache, weakness, drowsiness, dry mouth, increased thirst, muscle weakness, confusion, feeling tired or restless, nausea, vomiting, increased urination, constipation, muscle or bone pain, metallic taste in the mouth, loss of appetite, weight loss, itchy skin, changes in heart rate, unusual thoughts or behavior, problems with speech or balance, or severe pain in your upper stomach spreading to your back.
Avoid using food products that contain a fat substitute called olestra (Olean). Olestra can make it harder for your body to absorb cholecalciferol.
Avoid using antacids without your doctor's advice. Use only the specific type of antacid your doctor recommends.
Less serious side effects are more likely to occur, such as:
stomach pain or upset;
vomiting; or
constipation.
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.
The following drugs can interact with cholecalciferol, genistein, and zinc chelazome. Tell your doctor if you are using any of these:
cold medicine or throat lozenges that contain zinc;
cimetidine (Tagamet);
mineral oil;
orlistat (alli, Xenical);
seizure medication;
cholesterol-lowering medication such as cholestyramine (Prevalite, Questran), colesevelam (Welchol), colestipol (Colestid), eplerenone (Inspra), or spironolactone (Aldactazide, Aldactone); or
a diuretic (water pill) such as chlorothiazide (Diuril), hydrochlorothiazide (HCTZ, HydroDiuril, Hyzaar, Lopressor, Vasoretic, Zestoretic), chlorthalidone (Hygroton, Thalitone), indapamide (Lozol), metolazone (Mykrox, Zaroxolyn), and others.
This list is not complete and there may be other drugs that can interact with cholecalciferol, genistein, and zinc chelazome. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.
See also: cholecalciferol, genistein, and zinc chelazome side effects (in more detail)
Relieving runny nose; sneezing; itching of the nose or throat; itching, watery eyes; and cough caused by colds, upper respiratory infections, and allergies. It may also be used for other conditions as determined by your doctor.
Chlorcyclizine/Codeine Liquid is an antihistamine and narcotic cough suppressant combination. The antihistamine works by blocking the action of histamine, which helps reduce symptoms, such as watery eyes and sneezing. The cough suppressant works in the brain to help decrease the cough reflex, which reduces a dry cough.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Chlorcyclizine/Codeine Liquid. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Chlorcyclizine/Codeine Liquid. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if Chlorcyclizine/Codeine Liquid may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.
Use Chlorcyclizine/Codeine Liquid as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Chlorcyclizine/Codeine Liquid.
When used for long periods of time or at high doses, Chlorcyclizine/Codeine Liquid may not work as well and may require higher doses to obtain the same effect as when originally taken. This is known as TOLERANCE. Talk with your doctor if Chlorcyclizine/Codeine Liquid stops working as well. Do not take more than prescribed.
When used for long periods of time or at high doses, some people develop a need to continue taking Chlorcyclizine/Codeine Liquid. This is known as DEPENDENCE or addiction.
If you suddenly stop taking Chlorcyclizine/Codeine Liquid, you may experience WITHDRAWAL symptoms including anxiety; diarrhea; fever, runny nose, or sneezing; goose bumps and abnormal skin sensations; nausea; vomiting; pain; rigid muscles; rapid heartbeat; seeing, hearing, or feeling things that are not there; shivering or tremors; sweating; and trouble sleeping.
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:
Constipation; diarrhea; dizziness; drowsiness; dry mouth, nose, or throat; excitability; headache; loss of appetite; nausea; upset stomach; vomiting.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred vision, double vision, or other vision changes; confusion; difficulty urinating or inability to urinate; fast, slow, or irregular heartbeat; loss of coordination; mood or mental changes; nervousness; ringing in the ears; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; shallow breathing; tremor; trouble sleeping; uncontrolled muscle movements; unusual weakness or tiredness.
This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.
See also: Chlorcyclizine/Codeine side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (http://www.aapcc.org ), or emergency room immediately. Symptoms may include blurred vision; chest pain; cold or clammy skin; confusion; difficult or very slow breathing; hallucinations; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; unusually fast, slow, or irregular heartbeat; vomiting.
Store Chlorcyclizine/Codeine Liquid at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Chlorcyclizine/Codeine Liquid out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Chlorcyclizine/Codeine Liquid. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.
Antihistamine/Decongestant/Antitussive for oral use
For adults and pediatric patients (2 years and older)
Carbofed DM Syrup
Each teaspoonful (5 mL) contains brompheniramine maleate, 4 mg; pseudoephedrine hydrochloride, 45 mg; dextromethorphan hydrobromide, 15 mg.
Inactive ingredients: Citric acid, FD&C blue #1, FD&C red #33, glycerin, natural & artificial grape flavor, purified water, sodium benzoate, sodium citrate, sorbitol.
Brompheniramine maleate (2-Pyridinepropanamine, γ-(4-bromophenyl)-N,N-dimethyl-, (±)-, (Z)-2-butenedioate).
Pseudoephedrine hydrochloride (Benzenemethol, α-[1-methylamino)ethyl]-,[S-(R*,R*)]-, hydrochloride) is the hydrochloride of pseudoephedrine, a naturally occurring dextrorotatory stereoisomer of ephedrine.
Dextromethorphan hydrobromide (Morphinan, 3-methoxy-17-methyl-, (9α, 13α, 14α)-, hydrobromide monohydrate) is the hydrobromide of d-form race methorphan.
Antihistaminic, decongestant and antitussive actions.
Brompheniramine maleate possesses H1 antihistaminic activity and mild anticholinergic and sedative effects. Peak plasma concentration is reached in 5 hours. Urinary excretion is the major route of elimination. The liver is assumed to be the major site of metabolic transformation.
Pseudoephedrine hydrochloride is an oral sympathomimetic amine that acts as a decongestant to respiratory tract mucous membranes. While its vasoconstrictor action is similar to that of ephedrine, pseudoephedrine has less pressor effect in normotensive adults. Serum half-life for pseudoephedrine is 6 to 8 hours. Acidic urine is associated with faster elimination of the drug. About one-half of the administered dose is excreted in the urine.
Dextromethorphan hydrobromide is a nonnarcotic antitussive with effectiveness equal to codeine. It acts in the medulla oblongata to elevate the cough threshold. Dextromethorphan does not produce analgesia or induce tolerance, and has no potential for addiction. At usual doses, it will not depress respiration or inhibit ciliary activity. Dextromethorphan is rapidly metabolized with trace amounts of the parent compound in blood and urine. About onehalf of the administered dose is excreted in the urine as conjugated metabolites.
For relief of coughs and upper respiratory symptoms, including nasal congestion, associated with allergy or the common cold.
Patients with hypersensitivity or idiosyncrasy to any of its ingredients. Sympathomimetic amines are contraindicated in patients with severe hypertension, severe coronary artery disease and patients on monoamine oxidase (MAO) inhibitor therapy. Antihistamines are contraindicated in patients with narrow-angle glaucoma, urinary retention, peptic ulcer, and during an asthma attack. Dextromethorphan should not be used in patients receiving a monoamine oxidase inhibitor (MAOI) or for 2 weeks after stopping the MAOI drug.
Sympathomimetic amines should be used judiciously and sparingly in patients with hypertension, diabetes, ischemic heart disease, hyperthyroidism, increased intraocular pressure or prostatic hypertrophy. See CONTRAINDICATIONS. Sympathomimetic amines may produce CNS stimulation with convulsions or cardiovascular collapse with accompanying hypotension. The elderly (60 years and older) are more likely to exhibit adverse reactions. Antihistamines may cause excitability, especially in children. At doses higher than the recommended dose, nervousness, dizziness or sleeplessness may occur. Do not exceed recommended dosage. Administration of dextromethorphan may be accompanied by histamine release and should be used with caution in atopic children.
Before prescribing medication to suppress or modify cough, identify and provide therapy for the underlying cause of the cough and take caution that modification of cough does not increase the risk of clinical or physiologic complications. Dextromethorphan should be used with caution in sedated or debilitated patients and in patients confined to supine positions.
Use with caution in patients with hypertension, heart disease, asthma, hyperthyroidism, increased intraocular pressure, diabetes mellitus and prostatic hypertrophy.
Avoid alcohol and other CNS depressants while taking this product. Patients sensitive to antihistamines may experience moderate to severe drowsiness. Patients sensitive to sympathomimetics amines may note CNS stimulation.
Antihistamines may enhance the effects of tricyclic antidepressants, barbiturates, alcohol, and other CNS depressants. MAO inhibitors prolong and intensify the anticholinergic effects of antihistamines. Sympathomimetic amines may reduce the antihypertensive effects of reserpine, veratrum alkaloids, methyldopa and mecamylamine. Effects of sympathomimetics are increased with MAO inhibitors and beta-adrenergic blockers. The cough-suppressant action of dextromethorphan and narcotic antitussives are additive. Dextromethorphan is contraindicated with monoamine oxidase inhibitors (MAOI). (See CONTRAINDICATIONS section.)
Animal reproduction studies have not been concluded with Carbofed DM Syrup. It is not known whether these products can cause fetal harm when administered to a pregnant woman or affect reproductive capacity. Give to pregnant women only if clearly needed.
It is not known if the drugs in Carbofed DM Syrup are excreted in human milk. Since many drugs may be excreted into human milk and because of the potential for serious side effects in the nursing infant, this product should only be given to nursing mothers if clearly needed.
Safety and effectiveness of Carbofed DM Syrup in pediatric patients below the age of two years have not been established.
Antihistamines: Sedation, dizziness, diplopia, vomiting, diarrhea, dry mouth, headache, nervousness, nausea, anorexia, heartburn, weakness, polyuria and dysuria and, rarely, excitability in children. Urinary retention may occur in patients with prostatic hypertrophy.
Sympathomimetic amines: Convulsions, CNS stimulation, cardiac arrhythmia, respiratory difficulties, increased heart rate or blood pressure, hallucinations, tremors, nervousness, insomnia, pallor and dysuria.
Dextromethorphan: Drowsiness, dizziness, and GI disturbance.
To report SUSPECTED ADVERSE REACTIONS, contact Hi-Tech Pharmacal Co., Inc at 1-800-262-9010.
The signs, symptoms and treatment described below are those for H1 antihistamines, pseudoephedrine and dextromethorphan overdose.
The signs, symptoms and treatment described below are those for H1 antihistamines, pseudoephedrine and dextromethorphan overdose.
Should antihistamine effects predominate, central action constitutes the greatest danger. In the small child, predominate symptoms are excitation, hallucination, ataxia, incoordination, tremors, flushed face and fever. Convulsions, fixed and dilated pupils, coma and death may occur in severe cases. In the adult, fever and flushing are uncommon; excitement leading to convulsions and postictal depression is often preceded by drowsiness and coma. Respiration is usually not seriously depressed; blood pressure is usually stable.
Should sympathomimetic symptoms predominate, central effects include restlessness, dizziness, tremor, hyperactive reflexes, talkativeness, irritability and insomnia. Cardiovascular and renal effects include difficulty in micturition, headache, flushing, palpitation, cardiac arrhythmia, hypertension with subsequent hypotension and circulatory collapse. Gastrointestinal effects include dry mouth, metallic taste, anorexia, nausea, vomiting, diarrhea and abdominal cramps.
Dextromethorphan may cause respiratory depression with a large overdose.
a) Evacuate stomach as condition warrants. Activated charcoal may be useful.
b) Maintain a nonstimulated environment.
c) Monitor cardiovascular status.
d) Do not give stimulants.
e) Reduce fever with sponging.
f) Treat respiratory depression with naloxone if dextromethorphan toxicity is suspected.
g) Use sedatives or anticonvulsants to control CNS excitation and convulsions.
h) Physostigmine may reverse anticholinergic symptoms.
i) Ammonium chloride may acidify the urine to increase urinary excretion of pseudoephedrine.
j) Further care is symptomatic and supportive.
| ||
| AGE | DOSE* | FREQUENCY |
| 2-6 years | 1/2 teaspoonful (2.5 mL) | QID |
| adults and pediatric patients 6 years and over | 1 teaspoonful (5 mL) | QID |
Carbofed DM Syrup, grape flavored, in 16-fl-oz bottles. Dispense in USP tight, light-resistant, glass container. Store between 46º-86ºF (8º-30ºC). Avoid exposure to heat. Keep tightly closed.
Rx only.
Manufactured by:
Hi-Tech Pharmacal Co., Inc.
Amityville, NY 11701
Rev. 575:01 3/09
MG# 16623
NDC 50383-575-16
Carbofed DM Syrup
Antihistamine/Decongestant/Antitussive
Sugar Free • Alcohol Free
EACH 5mL (ONE TEASPOONFUL) CONTAINS:
Brompheniramine..........................................4 mg
Pseudoephedrine Hydrochloride..................45 mg
Dextromethorphan Hydrobromide...............15 mg
DOSAGE AND ADMINISTATION:
USUAL DOSAGE*:
2 to 6 years, 1/2 teaspoonful (2.5 mL), 4 times a day. Adults and pediatric patients 6 years and over, 1 teaspoonful (5 mL), 4 times a day.
*In mild cases or in particularly sensitive patients, less frequent or reduced doses may be adequate. See package insert for full prescribing information.
KEEP THIS AND ALL DRUGS OUT OF REACH OF CHILDREN.
In case of accidental overdose, seek professional assistance or contact a Poison Control Center Immediately.
IMPORTANT: Use safety closures when dispensing this product unless otherwise directed by the physician or requested by purchaser.
STORE BETWEEN 46°-86°F (8°-30°C)
AVOID EXPOSURE TO HEAT
CAP SEALED WITH BREAKAWAY BAND
DO NOT USE IF BROKEN OR MISSING
16 fl oz (473 mL)
HI-TECH PHARMACAL CO., INC.
Amityville, NY 11701
| Carbofed DM brompheniramine pseudoephedrine and dextromethorphan syrup | ||||||||||||||||||||||
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| Marketing Information | |||
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| Unapproved drug other | 09/03/2001 | 11/03/2011 | |
| Labeler - Hi-Tech Pharmacal Co., Inc. (101196749) |
Relieving itching, irritation, redness, dryness, scaling, and flaking of the skin caused by psoriasis. It may also be used for other conditions as determined by your doctor.
Coal Tar Foam is a keratolytic. It works by slowing bacterial growth and loosening and softening scales and crust.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Coal Tar Foam. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Coal Tar Foam. However, no specific interactions with Coal Tar Foam are known at this time.
Ask your health care provider if Coal Tar Foam may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.
Use Coal Tar Foam as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Coal Tar Foam.
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:
Itching, burning, tenderness, or redness; sensitivity to sunlight.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); irritation.
This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.
See also: Coal Tar side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.
Store Coal Tar Foam at room temperature, between 68 and 77 degrees F (20 and 25 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Do not expose to heat or store at temperatures above 120 degrees F (49 degrees C). Do not store in the bathroom. Do not puncture, break, or burn the canister even if it appears to be empty. Keep Coal Tar Foam out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Coal Tar Foam. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.
Generic Name: haemophilus b conjugate and hepatitis b vaccine (Intramuscular route)
hee-MOF-i-lus B KON-joo-gate VAX-een, hep-a-TYE-tis B VAX-een re-KOM-bin-ant
In the U.S.
Available Dosage Forms:
Therapeutic Class: Vaccine
Haemophilus b conjugate vaccine and hepatitis B vaccine is a combination immunizing agent that is used to prevent infection caused by the Haemophilus influenzae type b (Hib) bacteria and hepatitis B virus. The vaccine works by causing your body to produce its own protection (antibodies) against the disease.
Infections with Haemophilus influenza type b (Hib) bacteria can cause life-threatening illnesses, such as meningitis (a brain disease), epiglottitis (a throat disease that can cause suffocation), pericarditis (a heart disease), pneumonia (a lung disease), and septic arthritis (a bone and joint disease). Hib meningitis may cause death or leave the child with serious and permanent damage, such as mental retardation, deafness, epilepsy, or partial blindness.
HBV infection is a major cause of serious liver diseases, such as hepatitis and cirrhosis, and a type of liver cancer called primary hepatocellular carcinoma.
Pregnant women who have hepatitis B infection or are carriers of hepatitis B virus can give the disease to their babies when they are born. These babies often suffer serious long-term illnesses from the disease.
Immunization against hepatitis B disease is recommended for all newborn babies, infants, and young children.
This vaccine is to be administered only by or under the direct supervision of your doctor.
In deciding to use a vaccine, the risks of taking the vaccine must be weighed against the good it will do. This is a decision you and your doctor will make. For this vaccine, the following should be considered:
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.
Appropriate studies have not been performed on the relationship of age to the effects of Comvax® vaccine in infants younger than 6 weeks and older than 15 months of age. Safety and efficacy have not been established.
Comvax® vaccine is not recommended for adult or geriatric patients.
| Pregnancy Category | Explanation | |
|---|---|---|
| All Trimesters | C | Animal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women. |
There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.
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.
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.
The presence of other medical problems may affect the use of this vaccine. Make sure you tell your doctor if you have any other medical problems, especially:
A nurse or other trained health professional will give your child this vaccine. This vaccine is given as a shot into one of your child's muscles, usually in the thighs.
This vaccine is usually given as 3 doses. It is usually given at 2, 4, and 12 to 15 months of age, unless your child's doctor tells you otherwise.
It is important that your child receive all of the doses of vaccine in this series. Try to keep all of your scheduled appointments. If your child does miss a dose of this vaccine, make another appointment as soon as possible.
It is very important that your child return to your doctor’s office at the right time for the second and third dose. Be sure to notify your child's doctor of any unwanted effects that occur after he or she receives the vaccine.
If your child develops a skin rash, hives, or any allergic reaction after receiving this vaccine, tell your child's doctor right away.
Tell your child's doctor right away if your child is allergic to latex rubber. The vaccine vials may contain dry natural latex rubber. This may cause an allergic reaction in patients who are sensitive to latex.
Before your child have any medical tests, tell the medical doctor in charge that your child is receiving this vaccine. The results of some tests may be affected by this vaccine.
This vaccine may not protect your child against diseases caused by haemophilus influenzae type b or hepatitis B infection if your child is already infected with the virus at the time he or she receives the shot.
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 or nurse immediately if any of the following side effects occur:
Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:
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.
See also: Comvax side effects (in more detail)
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