Does PREGABALIN Cause Incorrect product administration duration? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Incorrect product administration duration have been filed in association with PREGABALIN (Pregabalin). This represents 0.0% of all adverse event reports for PREGABALIN.
23
Reports of Incorrect product administration duration with PREGABALIN
0.0%
of all PREGABALIN reports
4
Deaths
14
Hospitalizations
How Dangerous Is Incorrect product administration duration From PREGABALIN?
Of the 23 reports, 4 (17.4%) resulted in death, 14 (60.9%) required hospitalization, and 13 (56.5%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PREGABALIN. However, 23 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which PREGABALIN Alternatives Have Lower Incorrect product administration duration Risk?
PREGABALIN vs PREMARIN
PREGABALIN vs PREMPRO
PREGABALIN vs PRETOMANID
PREGABALIN vs PREVISCAN
PREGABALIN vs PREZISTA