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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 FORASEQ Cause Device malfunction? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device malfunction have been filed in association with FORASEQ. This represents 8.6% of all adverse event reports for FORASEQ.

8
Reports of Device malfunction with FORASEQ
8.6%
of all FORASEQ reports
0
Deaths
2
Hospitalizations

How Dangerous Is Device malfunction From FORASEQ?

Of the 8 reports, 2 (25.0%) required hospitalization.

Is Device malfunction Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for FORASEQ. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does FORASEQ Cause?

Dyspnoea (28) Asthma (16) Malaise (12) Fatigue (11) Drug ineffective (10) Pneumonia (10) Cough (9) Dysphonia (9) Pain (8) Chronic obstructive pulmonary disease (7)

What Other Drugs Cause Device malfunction?

PEGFILGRASTIM (6,818) EXENATIDE (3,273) BUDESONIDE\FORMOTEROL (2,771) ABATACEPT (2,459) SOMATROPIN (2,311) GOLIMUMAB (2,293) SECUKINUMAB (2,259) ALBUTEROL (2,257) GUSELKUMAB (1,410) MOMETASONE FUROATE (1,332)

Related Pages

FORASEQ Full Profile All Device malfunction Reports All Drugs Causing Device malfunction FORASEQ Demographics