Does LEVETIRACETAM Cause Product dose omission? 202 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 202 reports of Product dose omission have been filed in association with LEVETIRACETAM (Levetiracetam). This represents 0.3% of all adverse event reports for LEVETIRACETAM.
202
Reports of Product dose omission with LEVETIRACETAM
0.3%
of all LEVETIRACETAM reports
9
Deaths
96
Hospitalizations
How Dangerous Is Product dose omission From LEVETIRACETAM?
Of the 202 reports, 9 (4.5%) resulted in death, 96 (47.5%) required hospitalization, and 7 (3.5%) 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 LEVETIRACETAM. However, 202 reports have been filed with the FAERS database.
What Other Side Effects Does LEVETIRACETAM Cause?
Seizure (9,961)
Drug ineffective (8,666)
Off label use (5,789)
Maternal exposure during pregnancy (3,197)
Foetal exposure during pregnancy (2,604)
Epilepsy (2,546)
Generalised tonic-clonic seizure (2,276)
Somnolence (2,070)
Fatigue (1,972)
Status epilepticus (1,883)
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 LEVETIRACETAM Alternatives Have Lower Product dose omission Risk?
LEVETIRACETAM vs LEVOBUNOLOL
LEVETIRACETAM vs LEVOBUPIVACAINE
LEVETIRACETAM vs LEVOCARNITINE
LEVETIRACETAM vs LEVOCETIRIZINE
LEVETIRACETAM vs LEVODOPA