Does LAMOTRIGINE Cause Recalled product administered? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Recalled product administered have been filed in association with LAMOTRIGINE (Lamotrigine ER). This represents 0.0% of all adverse event reports for LAMOTRIGINE.
17
Reports of Recalled product administered with LAMOTRIGINE
0.0%
of all LAMOTRIGINE reports
1
Deaths
2
Hospitalizations
How Dangerous Is Recalled product administered From LAMOTRIGINE?
Of the 17 reports, 1 (5.9%) resulted in death, 2 (11.8%) required hospitalization, and 1 (5.9%) were considered life-threatening.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LAMOTRIGINE. However, 17 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which LAMOTRIGINE Alternatives Have Lower Recalled product administered Risk?
LAMOTRIGINE vs LANADELUMAB
LAMOTRIGINE vs LANADELUMAB-FLYO
LAMOTRIGINE vs LANREOTIDE
LAMOTRIGINE vs LANSOPRAZOLE
LAMOTRIGINE vs LANTHANUM