Methimazole interactions
Full monograph for MethimazoleCheck it against another medicine
Medicines
198 documented
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Clozapine | Major | Synergy | Case reports have suggested that concomitant use of clozapine and methimazole may result in acute granulocytopenia. The mechanism of this interaction is… | 5 sources — open the full entry |
| Deferiprone | Major | Synergy | Coadministration of deferiprone and other drugs that can cause neutropenia or agranulocytosis may increase the risk and/or severity of hematologic toxicity… | 5 sources — open the full entry |
| Fluphenazine + Nortriptyline | Major | Synergy | The concomitant use of fluphenazine and antithyroid agents may theoretically increase the risk of agranulocytosis. The mechanism of this interaction is unknown… | 1 sources — open the full entry |
| Fluphenazine Decanoate | Major | Synergy | The concomitant use of fluphenazine and antithyroid agents may theoretically increase the risk of agranulocytosis. The mechanism of this interaction is unknown… | 1 sources — open the full entry |
| Leflunomide | Major | Synergy | The recent, concomitant, or subsequent use (without the recommended leflunomide washout period or procedure) of other agents known to induce hepatotoxicity may… | 3 sources — open the full entry |
| Aminophylline | Moderate | Others | Clearance of theophylline and related agents depends upon thyroid function. In the hyperthyroid state, clearance may be enhanced. In the hypothyroid state… | 3 sources — open the full entry |
| Bimatoprost + Timolol | Moderate | Others | The clearance of some beta-blockers with high extraction ratios may be reduced when a euthyroid state is achieved after the addition of antithyroid agents… | 5 sources — open the full entry |
| Brimonidine Tartrate + Timolol Maleate | Moderate | Others | The clearance of some beta-blockers with high extraction ratios may be reduced when a euthyroid state is achieved after the addition of antithyroid agents… | 5 sources — open the full entry |
| Brinzolamide + Timolol | Moderate | Others | The clearance of some beta-blockers with high extraction ratios may be reduced when a euthyroid state is achieved after the addition of antithyroid agents… | 5 sources — open the full entry |
| Carvedilol | Moderate | Others | The clearance of some beta-blockers with high extraction ratios may be reduced when a euthyroid state is achieved after the addition of antithyroid agents… | 5 sources — open the full entry |
| Digoxin | Moderate | Excretion | The clearance of digitalis glycosides may be reduced when a euthyroid state is achieved after the addition of antithyroid agents. | 4 sources — open the full entry |
| Dorzolamide + Timolol | Moderate | Others | The clearance of some beta-blockers with high extraction ratios may be reduced when a euthyroid state is achieved after the addition of antithyroid agents… | 5 sources — open the full entry |
| Efavirenz | Moderate | Synergy | Coadministration of efavirenz with other agents known to induce hepatotoxicity may potentiate the risk of liver injury. Efavirenz has been associated with… | 7 sources — open the full entry |
| L-Asparginase | Moderate | Synergy | Concomitant use of asparaginase with other hepatotoxic agents may potentiate the risk of liver injury. Hepatomegaly, acute severe hepatotoxicity, and fatal… | 13 sources — open the full entry |
| Labetalol Hydrochloride | Moderate | Others | The clearance of some beta-blockers with high extraction ratios may be reduced when a euthyroid state is achieved after the addition of antithyroid agents… | 5 sources — open the full entry |
| Latanoprost + Timolol | Moderate | Others | The clearance of some beta-blockers with high extraction ratios may be reduced when a euthyroid state is achieved after the addition of antithyroid agents… | 5 sources — open the full entry |
| Levothyroxine Sodium | Moderate | Antagonism | Antithyroid agents such as methimazole and propylthiouracil can affect the therapeutic response to thyroid hormone therapy. These agents decrease thyroid… | 4 sources — open the full entry |
| Methotrexate | Moderate | Synergy | Coadministration of methotrexate with other agents known to induce hepatotoxicity may potentiate the risk of liver injury. Methotrexate, especially at higher… | 3 sources — open the full entry |
| Metoprolol Tartrate | Moderate | Others | The clearance of some beta-blockers with high extraction ratios may be reduced when a euthyroid state is achieved after the addition of antithyroid agents… | 5 sources — open the full entry |
| Prednisolone | Moderate | Metabolism | The clearance of prednisolone may be increased when coadministered with some antithyroid agents, such as carbimazole and methimazole. The mechanism for this… | 3 sources — open the full entry |
| Prednisolone + Neomycin Sulphate + Polymixin B Sulphate | Moderate | Metabolism | The clearance of prednisolone may be increased when coadministered with some antithyroid agents, such as carbimazole and methimazole. The mechanism for this… | 3 sources — open the full entry |
| Prednisolone Acetate | Moderate | Metabolism | The clearance of prednisolone may be increased when coadministered with some antithyroid agents, such as carbimazole and methimazole. The mechanism for this… | 3 sources — open the full entry |
| Propranolol Hydrochloride | Moderate | Others | The clearance of some beta-blockers with high extraction ratios may be reduced when a euthyroid state is achieved after the addition of antithyroid agents… | 5 sources — open the full entry |
| Remdesivir | Moderate | Synergy | Concomitant use of remdesivir with other agents that are known to induce hepatotoxicity may theoretically increase the risk of liver injury. Data from… | 5 sources — open the full entry |
| Theophylline | Moderate | Others | Clearance of theophylline and related agents depends upon thyroid function. In the hyperthyroid state, clearance may be enhanced. In the hypothyroid state… | 3 sources — open the full entry |
| Timolol Maleate | Moderate | Others | The clearance of some beta-blockers with high extraction ratios may be reduced when a euthyroid state is achieved after the addition of antithyroid agents… | 5 sources — open the full entry |
| Travoprost + Timolol Maleate | Moderate | Others | The clearance of some beta-blockers with high extraction ratios may be reduced when a euthyroid state is achieved after the addition of antithyroid agents… | 5 sources — open the full entry |
| Warfarin Sodium | Moderate | Others | Anticoagulation effects may be increased or decreased with the concomitant use of antithyroid drugs and vitamin K antagonists. The proposed mechanism may… | 49 sources — open the full entry |
| Phenobarbital | Minor | Absorption · Metabolism | Studies of rats have suggested that phenobarbital may cause a striking increase in the uptake and oxidation of methimazole in the thyroid. The clinical… | 1 sources — open the full entry |
Conditions
Conditions in which Methimazole needs care, as documented in this source.
Hematologic Diseases
MajorThe use of thioamide antithyroid agents may infrequently be associated with the development of blood dyscrasias, primarily agranulocytosis but also leukopenia, thrombocytopenia, and aplastic anemia. Most cases of agranulocytosis occur within the first two months of therapy, with incidence declining gradually thereafter. Patients older than 40 years of age and those receiving more than 40 mg/day of methimazole appear to be at substantially increased risk (a dosage association has not been reported for propylthiouracil). Therapy with thioamide derivatives should be administered cautiously in patients with or predisposed to blood dyscrasias and/or bone marrow depression. Clinical monitoring of hematopoietic function is recommended, with particular focus on leukocyte and differential counts. Because leukopenia (i.e. leukocyte count < 4000/mm3) may also occur in 10% of patients with untreated hyperthyroidism and is often associated with relative granulocytopenia, baseline count should be determined prior to initiating antithyroid medication. Patients should be instructed to immediately report during therapy any signs or symptoms suggestive of myelosuppression such as fever, sore throat, local infection, easy bruising, or bleeding. Cessation of antithyroid drug and institution of appropriate supportive measures are necessary if agranulocytosis or aplastic anemia develops.
10 sources
- Cooper DS "Antithyroid drugs." N Engl J Med 311 (1984): 1353-62
- Biswas N, Ahn YH, Goldman JM, Schwartz JM "Aplastic anemia associated with antithyroid drugs." Am J Med Sci 301 (1991): 190-4
- Valenta LJ, Elias AN, Weber DJ "Hyperthyroidism and propylthiouracil-induced agranulocytosis during chronic lithium carbonate therapy." Am J Psychiatry 138 (1981): 1605-7
- Shambaugh GE, 3d Khoury N, Zonschein J, Sizemore GW "Hypocalcemia accompanying agranulocytosis during propylthiouracil therapy." Ann Intern Med 91 (1979): 576-7
- Tajiri J, Noguchi S, Murakami T, Murakami N "Antithyroid drug-induced agranulocytosis. The usefulness of routine white blood cell count monitoring." Arch Intern Med 150 (1990): 621-4
- "Product Information. Propylthiouracil (propylthiouracil)." Lederle Laboratories (2001):
- Hoffman DM, Burgess J, Hill P "Agranulocytosis and hepatic dysfunction following propylthiouracil treatment." Aust N Z J Med 24 (1994): 409-10
- American Medical Association, Division of Drugs and Toxicology "Drug evaluations annual 1994." Chicago, IL: American Medical Association; (1994):
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- Bishara J, Cux S, Pitlik S "Methimazole-induced aplastic anemia." Ann Pharmacother 30 (1996): 684
- "Product Information. Tapazole (methimazole)." King Pharmaceuticals Inc (2001):
Hemorrhagic Disorders
MajorThioamide antithyroid agents may interfere with the action of vitamin K and have been reported in isolated cases to induce hypoprothombinemia and bleeding. Myelosuppression rarely resulting in thrombocytopenia has also been reported. Therapy with thioamide derivatives should be administered cautiously in patients with significant active bleeding or a hemorrhagic diathesis, including hemostatic and/or coagulation defects associated with hemophilia, vitamin K deficiency, hypoprothombinemia, thrombocytopenia, thrombocytopathy, or severe hepatic impairment. Clinical monitoring of prothrombin time or INR is recommended.
3 sources
- Sammon TJ, Peden VH, Witzleben C, King JP "Disseminated intravascular coagulation complicating propylthiouracil therapy. A case description of a 16-year-old girl." Clin Pediatr (Phila) 10 (1971): 739-42
- "Product Information. Propylthiouracil (propylthiouracil)." Lederle Laboratories (2001):
- "Product Information. Tapazole (methimazole)." King Pharmaceuticals Inc (2001):
Liver Diseases
MajorThe use of thioamide antithyroid agents has been associated with hepatotoxic effects, including transient elevations of serum transaminases and, rarely, cholestatic jaundice, fulminant hepatitis, hepatic necrosis, encephalopathy and death. Therapy with thioamide derivatives should be administered cautiously in patients with preexisting liver disease, a history of alcohol abuse, or hepatitis. Treatment should be discontinued if deterioration in liver function or other signs of hepatic injury occur. The jaundice associated with methimazole-induced hepatitis may persist for several weeks after withdrawal of the medication.
13 sources
- Limaye A, Ruffolo PR "Propylthiouracil-induced fatal hepatic necrosis." Am J Gastroenterol 82 (1987): 152-4
- Liaw YF, Huang MJ, Fan KD, Li KL, Wu SS, Chen TJ "Hepatic injury during propylthiouracil therapy in patients with hyperthyroidism. A cohort study." Ann Intern Med 118 (1993): 424-8
- Safani MM, Tatro DS, Rudd P "Fatal propylthiouracil-induced hepatitis ." Arch Intern Med 142 (1982): 838-9
- Hanson JS "Propylthiouracil and hepatitis. Two cases and a review of the literature." Arch Intern Med 144 (1984): 994-6
- Seidman DS, Livni E, Ilie B, Blum I "Propylthiouracil-induced cholestatic jaundice." J Toxicol Clin Toxicol 24 (1986): 353-60
- "Product Information. Propylthiouracil (propylthiouracil)." Lederle Laboratories (2001):
- Hoffman DM, Burgess J, Hill P "Agranulocytosis and hepatic dysfunction following propylthiouracil treatment." Aust N Z J Med 24 (1994): 409-10
- Westphal SA "Hepatotoxicity from propylthiouracil." South Med J 87 (1994): 943-7
Show all 13 sourcesShow fewer sources
- American Medical Association, Division of Drugs and Toxicology "Drug evaluations annual 1994." Chicago, IL: American Medical Association; (1994):
- Ozenirler S, Tuncer C, Boztepe U, Akyol G, Alkim H, Cakir N, Kandilci U "Propylthiouracil-induced hepatic damage." Ann Pharmacother 30 (1996): 960-3
- Deidiker R, Demello DE "Propylthiouracil-induced fulminant hepatitis: case report and review of the literature." Pediatr Pathol Lab Med 16 (1996): 845-52
- Hardee JT, Barnett AL, Thannoun A, Eghtesad B, Wheeler D, Jamal MM "Propylthiouracil-induced hepatotoxicity." West J Med 165 (1996): 144-7
- "Product Information. Tapazole (methimazole)." King Pharmaceuticals Inc (2001):