Does PREGABALIN Cause Product dose omission? 334 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 334 reports of Product dose omission have been filed in association with PREGABALIN (Pregabalin). This represents 0.3% of all adverse event reports for PREGABALIN.
334
Reports of Product dose omission with PREGABALIN
0.3%
of all PREGABALIN reports
1
Deaths
57
Hospitalizations
How Dangerous Is Product dose omission From PREGABALIN?
Of the 334 reports, 1 (0.3%) resulted in death, 57 (17.1%) required hospitalization, and 4 (1.2%) 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 PREGABALIN. However, 334 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?
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 PREGABALIN Alternatives Have Lower Product dose omission Risk?
PREGABALIN vs PREMARIN
PREGABALIN vs PREMPRO
PREGABALIN vs PRETOMANID
PREGABALIN vs PREVISCAN
PREGABALIN vs PREZISTA