Does LAMOTRIGINE Cause Product dose omission in error? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product dose omission in error have been filed in association with LAMOTRIGINE (Lamotrigine ER). This represents 0.0% of all adverse event reports for LAMOTRIGINE.
16
Reports of Product dose omission in error with LAMOTRIGINE
0.0%
of all LAMOTRIGINE reports
1
Deaths
6
Hospitalizations
How Dangerous Is Product dose omission in error From LAMOTRIGINE?
Of the 16 reports, 1 (6.3%) resulted in death, 6 (37.5%) required hospitalization, and 1 (6.3%) were considered life-threatening.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LAMOTRIGINE. However, 16 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 in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which LAMOTRIGINE Alternatives Have Lower Product dose omission in error Risk?
LAMOTRIGINE vs LANADELUMAB
LAMOTRIGINE vs LANADELUMAB-FLYO
LAMOTRIGINE vs LANREOTIDE
LAMOTRIGINE vs LANSOPRAZOLE
LAMOTRIGINE vs LANTHANUM