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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 COPAXONE Cause Product quality issue? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product quality issue have been filed in association with COPAXONE. This represents 1.0% of all adverse event reports for COPAXONE.

13
Reports of Product quality issue with COPAXONE
1.0%
of all COPAXONE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product quality issue From COPAXONE?

Of the 13 reports, 1 (7.7%) 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 COPAXONE. However, 13 reports have been filed with the FAERS database.

What Other Side Effects Does COPAXONE Cause?

Injection site pain (163) Multiple sclerosis relapse (136) Injection site reaction (116) Injection site mass (69) Injection site erythema (61) Dyspnoea (58) Death (50) Drug ineffective (45) Fatigue (42) Pain (40)

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 COPAXONE Alternatives Have Lower Product quality issue Risk?

COPAXONE vs COPEGUS COPAXONE vs COPPER COPAXONE vs CORDARONE COPAXONE vs CORICIDIN HBP COLD AND FLU COPAXONE vs CORTICOSTEROID NOS

Related Pages

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