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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 DUROGESIC Cause Product quality issue? 46 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 46 reports of Product quality issue have been filed in association with DUROGESIC. This represents 25.3% of all adverse event reports for DUROGESIC.

46
Reports of Product quality issue with DUROGESIC
25.3%
of all DUROGESIC reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product quality issue From DUROGESIC?

Of the 46 reports, 1 (2.2%) required hospitalization.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DUROGESIC. However, 46 reports have been filed with the FAERS database.

What Other Side Effects Does DUROGESIC Cause?

Wrong technique in drug usage process (63) Drug prescribing error (40) Inappropriate schedule of drug administration (24) Pain (18) Drug ineffective (15) Product adhesion issue (15) Overdose (12) Drug dose omission (9) Off label use (8) Breakthrough pain (7)

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 DUROGESIC Alternatives Have Lower Product quality issue Risk?

DUROGESIC vs DUROTEP MT DUROGESIC vs DURVALUMAB DUROGESIC vs DUTASTERIDE DUROGESIC vs DUTASTERIDE\TAMSULOSIN DUROGESIC vs DUVELISIB

Related Pages

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