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Methsuximide Disease Interactions

There are 4 disease interactions with methsuximide.

Major

Succinimides (applies to methsuximide) blood dyscrasias

Major Potential Hazard, Low plausibility. Applicable conditions: Bone Marrow Depression/Low Blood Counts

Hematologic toxicities, some with fatal outcome, have been associated with the use of succinimide anticonvulsants. Leukopenia, agranulocytosis, aplastic anemia, thrombocytopenia, pancytopenia, and eosinophilia have been reported. Therapy with succinimide anticonvulsants should be administered cautiously in patients with preexisting blood dyscrasias and/or bone marrow suppression. Complete blood counts, including platelets, should be performed prior to initiating therapy and periodically during therapy. Marked depression of blood counts may be indication for withdrawal of succinimide therapy.

References

  1. American Medical Association, Division of Drugs and Toxicology "Drug evaluations annual 1994." Chicago, IL: American Medical Association; (1994):
  2. Seip M "Aplastic anemia during ethosuximide medication. Treatment with bolus- methylprednisolone." Acta Paediatr Scand 72 (1983): 927-9
  3. Massey GV, Dunn NL, Heckel JL, Myer EC, Russell EC "Aplastic anemia following therapy for absence seizures with ethosuximide." Pediatr Neurol 11 (1994): 59-61
  4. "Product Information. Zarontin (ethosuximide)." Parke-Davis PROD (2001):
  5. "Product Information. Milontin (phensuximide)." Parke-Davis PROD (2001):
  6. "Product Information. Celontin (methsuximide)." Parke-Davis PROD
View all 6 references
Major

Succinimides (applies to methsuximide) renal/liver disease

Major Potential Hazard, Moderate plausibility. Applicable conditions: Renal Dysfunction

Succinimide anticonvulsants have produced morphological and functional changes in the liver of animals. In humans, abnormalities in liver and renal function studies have been reported. Therapy with succinimide anticonvulsants should be administered with extreme caution in patients with known hepatic or renal diseases. Periodic urinalysis and liver function tests are recommended for all patients treated with these drugs.

References

  1. Silverman SH, Gribetz D, Rausen AR "Nephrotic syndrome associated with ethosuccimide." Am J Dis Child 132 (1978): 99
  2. Coulter DL "Ethosuximide-induced liver dysfunction." Arch Neurol 40 (1983): 393-4
  3. Korinthenberg R, Wehrle L, Zimmerhackl LB "Renal tubular dysfunction following treatment with anti-epileptic drugs." Eur J Pediatr 153 (1994): 855-8
  4. "Product Information. Zarontin (ethosuximide)." Parke-Davis PROD (2001):
  5. "Product Information. Milontin (phensuximide)." Parke-Davis PROD (2001):
  6. "Product Information. Celontin (methsuximide)." Parke-Davis PROD
View all 6 references
Major

Succinimides (applies to methsuximide) SLE

Major Potential Hazard, Moderate plausibility. Applicable conditions: Lupus Erythematosus

Cases of systemic lupus erythematosus (SLE) have been reported in association with the use of succinimide anticonvulsants, primarily ethosuximide. Some of the patients recovered promptly following discontinuation of the drug, while others continued to have active disease long after. Therapy with succinimide anticonvulsants should be administered cautiously in patients with a history of SLE.

References

  1. Teoh PC, Chan HL "Lupus-scleroderma syndrome induced by ethosuximide." Arch Dis Child 50 (1975): 658-61
  2. Beernink DH, Miller JJ 3d "Anticonvulsant-induced antinuclear antibodies and lupus-like disease in children." J Pediatr 82 (1973): 113-7
  3. Alter BP "Systemic lupus erythematosus and ethosuccimide." J Pediatr 77 (1970): 1093-5
  4. Dabbous IA, Idriss HM "Occurrence of systemic lupus erythematosus in association with ethosuccimide therapy. Case report." J Pediatr 76 (1970): 617-20
  5. Livingston S, Rodriguez H, Greene CA, Pauli LL "Systemic lupus erythematosus. Occurrence in association with ethosuximide therapy." JAMA 203 (1968): 731-2
  6. Singsen BH, Fishman L, Hanson V "Antinuclear antibodies and lupus-like syndromes in children receiving anticonvulsants." Pediatrics 57 (1976): 529-34
  7. "Product Information. Zarontin (ethosuximide)." Parke-Davis PROD (2001):
  8. "Product Information. Milontin (phensuximide)." Parke-Davis PROD (2001):
  9. "Product Information. Celontin (methsuximide)." Parke-Davis PROD
View all 9 references
Moderate

Antiepileptics (applies to methsuximide) suicidal tendency

Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Depression, Psychosis

Antiepileptic drugs (AEDs) have been associated with an increased risk of suicidal thoughts or behavior in patients taking these drugs for any indication. Pooled analyses of 199 placebo-controlled clinical studies involving the use of 11 different AEDs showed that patients receiving AEDs had approximately twice the risk of suicidal thinking or behavior compared to patients receiving placebo. AEDs should be administered cautiously in patients with depression or other psychiatric disorders; phentermine-topiramate should be avoided in patients with history of suicidal attempts or active suicidal ideation. The risk of suicidal thoughts and behavior should be carefully assessed against the risk of untreated illness, bearing in mind that epilepsy and many other conditions for which AEDs are prescribed are themselves associated with morbidity and mortality and an increased risk of suicidal thoughts and behavior. Patients, caregivers, and families should be alert to the emergence or worsening of signs and symptoms of depression, any unusual changes in mood or behavior, or the emergence of suicidal thoughts or behavior. If patients have symptoms of suicidal ideation or behavior, a dosage reduction or treatment discontinuation should be considered.

References

  1. "Product Information. Tegretol (carbamazepine)." Novartis Pharmaceuticals PROD (2002):
  2. "Product Information. Klonopin (clonazepam)." Roche Laboratories PROD (2001):
  3. "Product Information. Dilantin (phenytoin)." Parke-Davis PROD (2001):
  4. "Product Information. Cerebyx (fosphenytoin)." Parke-Davis PROD (2001):
  5. "Product Information. Mysoline (primidone)." Elan Pharmaceuticals PROD (2001):
  6. "Product Information. Lyrica (pregabalin)." Pfizer U.S. Pharmaceuticals Group (2005):
  7. "Product Information. Sabril (vigabatrin)." Lundbeck Inc (2009):
  8. "Product Information. Potiga (ezogabine)." GlaxoSmithKline (2011):
  9. "Product Information. Fycompa (perampanel)." Eisai Inc (2012):
  10. "Product Information. Briviact (brivaracetam)." UCB Pharma Inc (2016):
  11. "Product Information. Epidiolex (cannabidiol)." Greenwich Biosciences LLC (2018):
  12. "Product Information. Xcopri (cenobamate)." SK Life Science, Inc. (2020):
  13. "Product Information. Fintepla (fenfluramine)." Zogenix, Inc (2020):
  14. "Product Information. Ztalmy (ganaxolone)." Marinus Pharmaceuticals, Inc (2022):
  15. "Product Information. Diacomit (stiripentol)." Biocodex USA SUPPL-3 (2022):
  16. "Product Information. Qsymia (phentermine-topiramate)." Vivus Inc SUPPL-23 (2023):
  17. "Product Information. Topamax (topiramate)." Janssen Pharmaceuticals SUPPL-65 (2023):
View all 17 references

Methsuximide drug interactions

There are 246 drug interactions with methsuximide.

Methsuximide alcohol/food interactions

There is 1 alcohol/food interaction with methsuximide.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.