Does PREGABALIN Cause Product dose omission in error? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Product dose omission in error have been filed in association with PREGABALIN (Pregabalin). This represents 0.0% of all adverse event reports for PREGABALIN.
32
Reports of Product dose omission in error with PREGABALIN
0.0%
of all PREGABALIN reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product dose omission in error From PREGABALIN?
Of the 32 reports, 4 (12.5%) required hospitalization.
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 PREGABALIN. However, 32 reports have been filed with the FAERS database.
What Other Side Effects Does PREGABALIN Cause?
Drug ineffective (13,664)
Pain (12,996)
Malaise (6,320)
Dizziness (5,878)
Off label use (5,713)
Somnolence (5,528)
Pain in extremity (5,023)
Fatigue (4,909)
Weight increased (4,903)
Condition aggravated (4,901)
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 PREGABALIN Alternatives Have Lower Product dose omission in error Risk?
PREGABALIN vs PREMARIN
PREGABALIN vs PREMPRO
PREGABALIN vs PRETOMANID
PREGABALIN vs PREVISCAN
PREGABALIN vs PREZISTA