Does DURAGESIC Cause Product quality issue? 175 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 175 reports of Product quality issue have been filed in association with DURAGESIC. This represents 41.3% of all adverse event reports for DURAGESIC.
175
Reports of Product quality issue with DURAGESIC
41.3%
of all DURAGESIC reports
1
Deaths
32
Hospitalizations
How Dangerous Is Product quality issue From DURAGESIC?
Of the 175 reports, 1 (0.6%) resulted in death, 32 (18.3%) 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 DURAGESIC. However, 175 reports have been filed with the FAERS database.
What Other Side Effects Does DURAGESIC Cause?
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)
Therapeutic response decreased (26)
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 DURAGESIC Alternatives Have Lower Product quality issue Risk?
DURAGESIC vs DUROGESIC
DURAGESIC vs DUROTEP MT
DURAGESIC vs DURVALUMAB
DURAGESIC vs DUTASTERIDE
DURAGESIC vs DUTASTERIDE\TAMSULOSIN