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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 DAYTRANA Cause Product quality issue? 747 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 747 reports of Product quality issue have been filed in association with DAYTRANA. This represents 51.6% of all adverse event reports for DAYTRANA.

747
Reports of Product quality issue with DAYTRANA
51.6%
of all DAYTRANA reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product quality issue From DAYTRANA?

Of the 747 reports.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DAYTRANA. However, 747 reports have been filed with the FAERS database.

What Other Side Effects Does DAYTRANA Cause?

No adverse event (580) Wrong technique in drug usage process (376) Off label use (306) Incorrect drug administration duration (287) Application site erythema (263) Drug prescribing error (240) Drug administration error (204) Drug ineffective (182) Drug administered at inappropriate site (141) Application site pruritus (122)

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 DAYTRANA Alternatives Have Lower Product quality issue Risk?

DAYTRANA vs DECITABINE DAYTRANA vs DEFERASIROX DAYTRANA vs DEFERIPRONE DAYTRANA vs DEFEROXAMINE DAYTRANA vs DEFIBROTIDE

Related Pages

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