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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 DURAGESIC Cause Adverse event? 23 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Adverse event have been filed in association with DURAGESIC. This represents 5.4% of all adverse event reports for DURAGESIC.

23
Reports of Adverse event with DURAGESIC
5.4%
of all DURAGESIC reports
1
Deaths
7
Hospitalizations

How Dangerous Is Adverse event From DURAGESIC?

Of the 23 reports, 1 (4.3%) resulted in death, 7 (30.4%) required hospitalization.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DURAGESIC. However, 23 reports have been filed with the FAERS database.

What Other Side Effects Does DURAGESIC Cause?

Product quality issue (175) Wrong technique in drug usage process (172) Drug dose omission (141) Product adhesion issue (102) Drug ineffective (82) Pain (69) Inappropriate schedule of drug administration (43) Hyperhidrosis (33) Malaise (33) Drug administered at inappropriate site (26)

What Other Drugs Cause Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which DURAGESIC Alternatives Have Lower Adverse event Risk?

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

Related Pages

DURAGESIC Full Profile All Adverse event Reports All Drugs Causing Adverse event DURAGESIC Demographics