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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does LAMOTRIGINE Cause Product dose omission? 115 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 115 reports of Product dose omission have been filed in association with LAMOTRIGINE (Lamotrigine ER). This represents 0.2% of all adverse event reports for LAMOTRIGINE.

115
Reports of Product dose omission with LAMOTRIGINE
0.2%
of all LAMOTRIGINE reports
10
Deaths
44
Hospitalizations

How Dangerous Is Product dose omission From LAMOTRIGINE?

Of the 115 reports, 10 (8.7%) resulted in death, 44 (38.3%) required hospitalization.

Is Product dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LAMOTRIGINE. However, 115 reports have been filed with the FAERS database.

What Other Side Effects Does LAMOTRIGINE Cause?

Drug ineffective (5,175) Seizure (3,459) Toxicity to various agents (3,256) Rash (3,249) Foetal exposure during pregnancy (2,985) Off label use (2,625) Completed suicide (2,433) Drug reaction with eosinophilia and systemic symptoms (2,235) Dizziness (2,170) Pyrexia (1,967)

What Other Drugs Cause Product dose omission?

APREMILAST (4,567) DUPILUMAB (2,729) ALBUTEROL (1,742) USTEKINUMAB (1,653) INSULIN GLARGINE (1,500) ETANERCEPT (1,400) LENALIDOMIDE (1,400) RUXOLITINIB (1,376) ALIROCUMAB (1,354) DIMETHYL (1,248)

Which LAMOTRIGINE Alternatives Have Lower Product dose omission Risk?

LAMOTRIGINE vs LANADELUMAB LAMOTRIGINE vs LANADELUMAB-FLYO LAMOTRIGINE vs LANREOTIDE LAMOTRIGINE vs LANSOPRAZOLE LAMOTRIGINE vs LANTHANUM

Related Pages

LAMOTRIGINE Full Profile All Product dose omission Reports All Drugs Causing Product dose omission LAMOTRIGINE Demographics