Does LACOSAMIDE Cause Product dose omission? 180 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 180 reports of Product dose omission have been filed in association with LACOSAMIDE (Lacosamide). This represents 0.9% of all adverse event reports for LACOSAMIDE.
180
Reports of Product dose omission with LACOSAMIDE
0.9%
of all LACOSAMIDE reports
8
Deaths
97
Hospitalizations
How Dangerous Is Product dose omission From LACOSAMIDE?
Of the 180 reports, 8 (4.4%) resulted in death, 97 (53.9%) required hospitalization, and 5 (2.8%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LACOSAMIDE. However, 180 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?
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 LACOSAMIDE Alternatives Have Lower Product dose omission Risk?
LACOSAMIDE vs LACTOBACILLUS ACIDOPHILUS
LACOSAMIDE vs LACTOBACILLUS RHAMNOSUS
LACOSAMIDE vs LACTOSE
LACOSAMIDE vs LACTULOSE
LACOSAMIDE vs LAMICTAL