Does LACOSAMIDE Cause Product dose omission issue? 191 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 191 reports of Product dose omission issue have been filed in association with LACOSAMIDE (Lacosamide). This represents 0.9% of all adverse event reports for LACOSAMIDE.
191
Reports of Product dose omission issue with LACOSAMIDE
0.9%
of all LACOSAMIDE reports
10
Deaths
68
Hospitalizations
How Dangerous Is Product dose omission issue From LACOSAMIDE?
Of the 191 reports, 10 (5.2%) resulted in death, 68 (35.6%) required hospitalization, and 4 (2.1%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LACOSAMIDE. However, 191 reports have been filed with the FAERS database.
What Other Side Effects Does LACOSAMIDE Cause?
Seizure (4,585)
Drug ineffective (2,945)
Off label use (2,811)
Dizziness (974)
Overdose (971)
Generalised tonic-clonic seizure (918)
Epilepsy (902)
Status epilepticus (874)
Fall (780)
Somnolence (768)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which LACOSAMIDE Alternatives Have Lower Product dose omission issue Risk?
LACOSAMIDE vs LACTOBACILLUS ACIDOPHILUS
LACOSAMIDE vs LACTOBACILLUS RHAMNOSUS
LACOSAMIDE vs LACTOSE
LACOSAMIDE vs LACTULOSE
LACOSAMIDE vs LAMICTAL