Ketoderm may be available in the countries listed below.
Ingredient matches for Ketoderm
Ketoconazole is reported as an ingredient of Ketoderm in the following countries:
- Algeria
- Canada
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Ketoderm may be available in the countries listed below.
Ketoconazole is reported as an ingredient of Ketoderm in the following countries:
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Elcion may be available in the countries listed below.
Diazepam is reported as an ingredient of Elcion in the following countries:
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Evidon may be available in the countries listed below.
Tocopherol, α- is reported as an ingredient of Evidon in the following countries:
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Desal may be available in the countries listed below.
Furosemide is reported as an ingredient of Desal in the following countries:
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Muscalm D may be available in the countries listed below.
Tolperisone hydrochloride (a derivative of Tolperisone) is reported as an ingredient of Muscalm D in the following countries:
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Virtaz may be available in the countries listed below.
Aciclovir is reported as an ingredient of Virtaz in the following countries:
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Prisulfan may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Sulfadiazine is reported as an ingredient of Prisulfan in the following countries:
Trimethoprim is reported as an ingredient of Prisulfan in the following countries:
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In some countries, this medicine may only be approved for veterinary use.
Monensin sodium salt (a derivative of Monensin) is reported as an ingredient of Moormans in the following countries:
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Heptodin may be available in the countries listed below.
Lamivudine is reported as an ingredient of Heptodin in the following countries:
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Aspirin Protect may be available in the countries listed below.
Acetylsalicylic Acid is reported as an ingredient of Aspirin Protect in the following countries:
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Vitamin E AL may be available in the countries listed below.
Tocopherol, α- is reported as an ingredient of Vitamin E AL in the following countries:
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Kosozole may be available in the countries listed below.
Albendazole is reported as an ingredient of Kosozole in the following countries:
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Mirtazapina Mylan may be available in the countries listed below.
Mirtazapine is reported as an ingredient of Mirtazapina Mylan in the following countries:
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Risperidon-neuraxpharm may be available in the countries listed below.
Risperidone is reported as an ingredient of Risperidon-neuraxpharm in the following countries:
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Class: Antihistamines
ATC Class: A04AD
CAS Number: 523-87-5
Brands: DMH, Dramamine, TripTone
Ethanolamine-derivative antihistamine containing a diphenhydramine moiety; antiemetic.b
Used principally in the prevention and treatment of nausea, vomiting, and/or vertigo associated with motion sickness, although scopolamine, promethazine, or meclizine may be more effective.b
Most effective when given prophylactically.b
Has been used for symptomatic treatment (e.g., nausea, vomiting, vertigo) of Ménière’s disease† and other vestibular disturbances†.b
May be less effective than phenothiazines in controlling nausea and vomiting not related to vestibular stimulation.b
Although a histamine antagonist, use in allergic conditions† has not been evaluated.b
Administer orally or by IM or IV injection.a b
Each 50 mg must be diluted with 10 mL of 0.9% sodium chloride injection.b
Inject IV slowly over a period of 2 minutes.b
For prevention, take 30 minutes before exposure to motion.b
Children <2 Years of Age: Give only under the direction of a clinician.100 101
Children 2 to <6 Years of Age: 12.5–25 mg every 6–8 hours, not to exceed 75 mg in 24 hours, or as directed by a clinician.100 101 102
Children 6 to <12 Years of Age: 25–50 mg every 6–8 hours, not to exceed 150 mg in 24 hours, or as directed by a clinician.100 101 102
Children ≥12 Years of Age: Usually, 50–100 mg every 4–6 hours, not to exceed 400 mg in 24 hours, or as directed by a clinician.100 101 102
Children: Alternatively, 1.25 mg/kg or 37.5 mg/m2 4 times daily, up to a maximum of 300 mg daily.b
Children: 1.25 mg/kg or 37.5 mg/m2 4 times daily, up to a maximum of 300 mg daily.b
Not established for children.b
For prevention, take 30 minutes before exposure to motion.b
Usually 50–100 mg every 4–6 hours, not to exceed 400 mg in 24 hours, or as directed by a clinician.100 101 102
50–100 mg every 4–6 hours, not to exceed 400 mg in 24 hours, or as directed by a clinician.b
50–100 mg every 4–6 hours, not to exceed 400 mg in 24 hours, or as directed by a clinician.b
25–50 mg has been given 3 times daily.b
50 mg.b
Children 2 to <6 Years of Age: Maximum 75 mg in 24 hours, or as directed by a clinician.100 101 102
Children 6 to <12 Years of Age: Maximum 150 mg in 24 hours, or as directed by a clinician.100 101 102
Children ≥12 Years of Age: Maximum 400 mg in 24 hours, or as directed by a clinician.100 101 102
Children: Alternatively, maximum 300 mg daily when given as 1.25 mg/kg or 37.5 mg/m2.b
300 mg daily.b
Maximum 400 mg in 24 hours, or as directed by a clinician.100 101 102
Maximum 400 mg in 24 hours, or as directed by a clinician.b
Maximum 400 mg in 24 hours, or as directed by a clinician.b
No specific dosage recommendations for hepatic impairment.a b
No specific dosage recommendations for renal impairment.a b
No specific geriatric dosage recommendations.a
Dimenhydrinate contains 53–55.5% diphenhydramine.a b Concomitant use with other preparations containing diphenhydramine, including oral and topical preparations, is contraindicated.
Known hypersensitivity to dimenhydrinate, other antihistamines with similar chemical structure, or any ingredient in the formulation.
Patients with glaucoma, respiratory conditions (e.g., emphysema, chronic bronchitis), or difficulty urinating due to prostatic hypertrophy should consult a clinician before initiating therapy with dimenhydrinate.a b
Use with caution in patients with increased IOP, narrow-angle glaucoma, stenosing peptic ulcer, pyloroduodenal obstruction, bladder-neck obstruction, symptomatic prostatic hypertrophy, active or a history of lower respiratory disease (e.g., bronchial asthma), hyperthyroidism, or cardiovascular disease (e.g., hypertension).a b
Risk of marked drowsiness.c Among first generation antihistamines, ethanolamines (e.g., dimenhydrinate) considered the most sedating.c
Performance of activities requiring mental alertness or physical coordination may be impaired.a b
Concurrent use of other CNS depressants may cause additive or potentiated CNS depression.a
Dimenhydrinate contains 53–55.5% diphenhydramine.a b Risk of diphenhydramine toxicity. (See Pediatric Use under Cautions.) Do not use more often than directed for any condition or use concomitantly with other diphenhydramine-containing preparations, including oral and topical preparations.
Dramamine chewable tablets contain tartrazine (FD&C yellow No. 5), which may cause allergic reactions including bronchial asthma in susceptible individuals.a b Incidence of tartrazine sensitivity is low, but it frequently occurs in patients who are sensitive to aspirin.b
Consider anticholinergic effects in patients with conditions aggravated by anticholinergic therapy (e.g., angle-closure glaucoma, enlargement of the prostate gland).b (See Concomitant Diseases under Cautions.)
Symptoms of ototoxicity may be masked by dimenhydrinate; administer with caution in patients receiving known ototoxic drugs and closely monitor.b
Use with caution in seizure disorders.b
Category C.pdh
Distributed into milk.b Discontinue nursing or the drug.b
Do not use in children <2 years of age unless directed by a clinician.a
Risk of diminished mental alertness. Risk of excitation in young pediatric patients.b
Risk of diphenhydramine toxicity (e.g., dilated pupils, flushed face, hallucinations, ataxic gait, urinary retention) when used concomitantly with other diphenhydramine-containing preparations, including oral and topical preparations. (See Diphenhydramine Toxicity under Cautions.)
Drowsiness, headache, blurred vision, tinnitus, dryness of the mouth and respiratory passages, incoordination, palpitation, dizziness, hypotension.b
Paradoxical CNS stimulation in pediatric patients and occasionally in adults.b
With IM injection: Pain at the injection site.b
Because dimenhydrinate contains diphenhydramine, the possibility of other diphenhydramine-related adverse effects should also be considered.b
Although dimenhydrinate has been reported to induce hepatic microsomal enzymes in animals, there is no clinical evidence that it influences the metabolism of other drugs in humans.b
Drug | Interaction | Comments |
|---|---|---|
Anticholinergic drugs | Anticholinergic effects may be potentiatedb | |
Antidepressants, tricyclic | Anticholinergic effects may be potentiatedb | |
CNS depressants | May enhance the effects of other CNS depressants, including alcoholb | Use concomitantly with cautionb |
Ototoxic drugs | May mask the early manifestations of ototoxicityb | Use concomitantly with caution and closely monitorb |
Well absorbed after oral or parenteral administration.b
IV injection: Antiemetic effects occur almost immediately.b
Oral administration: Antiemetic effects within 15–30 minutes.b
IM injection: Antiemetic effects within 20–30 minutes.b
3–6 hours.b
Probably widely distributed into body tissues.b
Crosses the placenta.b
Small amounts are distributed into milk.b
Metabolized by the liver.b
Excreted in urine.b
Well-closed containers at room temperature.b d
Tight containers.b d Avoid freezing.b
Well-closed containers at room temperature.b d
Avoid freezing.b
For information on systemic interactions resulting from concomitant use, see Interactions.
Compatible |
|---|
Dextran 6% in dextrose 5% |
Dextran 6% in sodium chloride 0.9% |
Dextrose–Ringer’s injection combinations |
Dextrose–Ringer’s injection, lactated, combinations |
Dextrose–saline combinations |
Dextrose 5% in sodium chloride 0.9% |
Dextrose 2.5, 5, or 10% in water |
Fructose 10% in sodium chloride 0.9% |
Fructose 10% in water |
Invert sugar 5 and 10% in sodium chloride 0.9% |
Invert sugar 5 and 10% in water |
Ionosol products |
Ringer’s injection |
Ringer’s injection, lactated |
Sodium chloride 0.45 or 0.9% |
Sodium lactate (1/6) M |
Compatible |
|---|
Amikacin sulfate |
Calcium gluconate |
Chloramphenicol sodium succinate |
Heparin sodium |
Hydroxyzine HCl |
Norepinephrine bitartrate |
Penicillin G potassium |
Pentobarbital sodium |
Phenobarbital sodium |
Potassium chloride |
Prochlorperazine edisylate |
Vancomycin HCl |
Vitamin B complex with C |
Incompatible |
Thiopental sodium |
Variable |
Aminophylline |
Ammonium chloride |
Amobarbital sodium |
Hydrocortisone sodium succinate |
Compatible |
|---|
Acyclovir sodium |
Ciprofloxacin |
Fluconazole |
Metronidazole |
Pantoprazole sodium |
Most actions are believed to result principally from its diphenhydramine moiety.b
Has CNS depressant, anticholinergic, antiemetic, antihistaminic, and local anesthetic effects.b
Has been shown to inhibit vestibular stimulation, acting first on the otolith system, and in larger doses on the semicircular canals.b
Inhibits acetylcholine; this may be its primary mechanism of action, since cholinergic stimulation in the vestibular and reticular systems may be responsible for the nausea and vomiting of motion sickness.b
Tolerance to CNS depressant effects usually occurs after a few days of treatment, and some decrease in antiemetic effectiveness may be noted after prolonged use.b
Potential for drug to impair mental alertness or physical coordination; avoid driving or operating machinery until effects on individual are known.a b
Importance of warning patients with tartrazine or aspirin sensitivity that Dramamine chewable tablets contain the dye tartrazine (FD&C yellow No. 5), which may cause allergic reactions including bronchial asthma.a b .
Importance of not using multiple diphenhydramine-containing preparations (either oral or topical) simultaneously because of risk of toxicity. (See Diphenhydramine Toxicity under Cautions.)
Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs as well as any concomitant illnesses.
Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.
Importance of informing patients of other important precautionary information. (See Cautions.)
Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.
* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name
Routes | Dosage Forms | Strengths | Brand Names | Manufacturer |
|---|---|---|---|---|
Oral | Solution | 12.5 mg/5 mL* | DMH Syrup | Alra |
Dramamine Children’s (with methylparaben) | Pfizer | |||
Tablets | 50 mg* | Dramamine (scored) | Pfizer | |
Tablets, chewable | 50 mg | Dramamine Children’s (with sorbitol and tartrazine; scored) | Pfizer | |
Tablets, film-coated | 50 mg | TripTone Caplets (scored) | Del | |
Parenteral | Injection | 50 mg/mL* | Dimenhydrinate Injection (with propylene glycol and benzyl alcohol) | Abraxis |
This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.
The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.
AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions August 2007. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.
† Use is not currently included in the labeling approved by the US Food and Drug Administration.
Only references cited for selected revisions after 1984 are available electronically.
100. Food and Drug Administration. Antiemetic drug products for over-the-counter human use; final monograph. Fed Regist. 1987; 52:15886-93.
101. Richardson-Vicks Inc. Dramamine Liquid, Dramamine tablets, and Dramamine Chewable tablets prescribing information. In: Huff BB, ed. Physicians’ desk reference. 42nd ed. Oradell, NJ: Medical Economics Company Inc; 1988(Suppl A):A30-1.
102. Food and Drug Administration. Over-the-counter drug products; final monographs for antiemetic, antitussive, bronchodilator, and antihelmintic drug products; updating and technical changes Fed Regist. 1988; 53:35808-10. (21 CFR Parts 336, 341, and 357 [Docket No. 88N-0070])
556. Food and Drug Administration. Labeling of diphenhydramine-containing drug products for over-the-counter human use. 21 CFR Parts 336, 338, 341, 348. Proposed rule. [Docket No. 97N-0128] Fed Regist. 1997; 62:45767-74.
557. Chan CYJ, Wallander KA. Diphenhydramine toxicity in three children with varicella- zoster infection. DICP. 1991; 25:130-2. [IDIS 278321] [PubMed 2058184]
575. McGann KP, Pribanich S, Graham JA et al. Diphenhydramine toxicity in a child with varicella: a case report. J Fam Pract. 1992; 35:210,213-4. [PubMed 1645115]
576. Woodward GA, Baldassano RN. Topical diphenhydramine toxicity in a five year old with varicella. Pediatr Emerg Care. 1988; 4:18-20. [PubMed 3362727]
672. Food and Drug Administration. Labeling of diphenhydramine-containing drug products for over-the-counter human use. 21 CFR Parts 336, 338, 341, 348. Final rule. [Docket No. 97N-0128] Fed Regist. 2002; 67:72555-9.
a. Pharmacia Consumer Healthcare. Dramamine (dimenhydrinate) Original Formula and Chewable tablets prescribing information. Peapack, NJ: 2004 Apr.
b. AHFS drug information 2004. McEvoy GK, ed. Dimenhydrinate. American Society of Health-System Pharmacists; 2004: 2786-7.
c. AHFS drug information 2004. McEvoy GK, ed. Antihistamines general statement. American Society of Health-System Pharmacists; 2004:2-9.
d. The United States pharmacopeia, 27th rev, and The national formulary, 22nd ed. Rockville, MD: The United States Pharmacopeial Convention, Inc; 2004:10,628-31.
pdh. Schilling McCann JA, Publisher. Pharmacists drug handbook. 2nd ed. Philadelphia, PA: Lippincott Williams and Wilkins and American Society of Health-System Pharmacists; 2003.
HID. Trissel LA. Handbook on injectable drugs. 14th ed. Bethesda, MD: American Society of Health-System Pharmacists; 2007:529-35.
In some countries, this medicine may only be approved for veterinary use.
Oxytetracycline is reported as an ingredient of Tetroxy in the following countries:
Oxytetracycline dihydrate (a derivative of Oxytetracycline) is reported as an ingredient of Tetroxy in the following countries:
Oxytetracycline hydrochloride (a derivative of Oxytetracycline) is reported as an ingredient of Tetroxy in the following countries:
Oxytetracycline magnesiumoxyethylammonium (a derivative of Oxytetracycline) is reported as an ingredient of Tetroxy in the following countries:
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Propantheline Bromide Lisheng Pharm may be available in the countries listed below.
Propantheline Bromide is reported as an ingredient of Propantheline Bromide Lisheng Pharm in the following countries:
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Efetrin may be available in the countries listed below.
Venlafaxine hydrochloride (a derivative of Venlafaxine) is reported as an ingredient of Efetrin in the following countries:
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