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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does PREDNICARBATE Cause Product quality issue? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product quality issue have been filed in association with PREDNICARBATE. This represents 10.8% of all adverse event reports for PREDNICARBATE.

12
Reports of Product quality issue with PREDNICARBATE
10.8%
of all PREDNICARBATE reports
11
Deaths
11
Hospitalizations

How Dangerous Is Product quality issue From PREDNICARBATE?

Of the 12 reports, 11 (91.7%) resulted in death, 11 (91.7%) required hospitalization, and 11 (91.7%) were considered life-threatening.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PREDNICARBATE. However, 12 reports have been filed with the FAERS database.

What Other Side Effects Does PREDNICARBATE Cause?

Drug ineffective (55) Paraesthesia (50) Vomiting (50) Blepharospasm (49) Epilepsy (49) Gastrooesophageal reflux disease (49) Hypoaesthesia (49) Memory impairment (49) Abdominal pain upper (48) Drug intolerance (48)

What Other Drugs Cause Product quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which PREDNICARBATE Alternatives Have Lower Product quality issue Risk?

PREDNICARBATE vs PREDNISOLONE PREDNICARBATE vs PREDNISOLONE METAZOATE PREDNICARBATE vs PREDNISOLONE\PREDNISOLONE\PREDNISOLONE PREDNICARBATE vs PREDNISONE PREDNICARBATE vs PREGABALIN

Related Pages

PREDNICARBATE Full Profile All Product quality issue Reports All Drugs Causing Product quality issue PREDNICARBATE Demographics