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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 Product packaging quantity issue? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product packaging quantity issue have been filed in association with DURAGESIC. This represents 3.1% of all adverse event reports for DURAGESIC.

13
Reports of Product packaging quantity issue with DURAGESIC
3.1%
of all DURAGESIC reports
0
Deaths
4
Hospitalizations

How Dangerous Is Product packaging quantity issue From DURAGESIC?

Of the 13 reports, 4 (30.8%) required hospitalization.

Is Product packaging quantity issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DURAGESIC. However, 13 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 Product packaging quantity issue?

LEUPROLIDE (523) ALBUTEROL (431) BUDESONIDE\FORMOTEROL (301) FENTANYL (286) BUPRENORPHINE (225) CYCLOSPORINE (206) ESTRADIOL (201) BIMATOPROST (177) RIVAROXABAN (174) EXENATIDE (154)

Which DURAGESIC Alternatives Have Lower Product packaging quantity issue Risk?

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

Related Pages

DURAGESIC Full Profile All Product packaging quantity issue Reports All Drugs Causing Product packaging quantity issue DURAGESIC Demographics