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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 ATOGEPANT Cause Product use complaint? 19 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Product use complaint have been filed in association with ATOGEPANT (Qulipta). This represents 0.4% of all adverse event reports for ATOGEPANT.

19
Reports of Product use complaint with ATOGEPANT
0.4%
of all ATOGEPANT reports
0
Deaths
3
Hospitalizations

How Dangerous Is Product use complaint From ATOGEPANT?

Of the 19 reports, 3 (15.8%) required hospitalization.

Is Product use complaint Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ATOGEPANT. However, 19 reports have been filed with the FAERS database.

What Other Side Effects Does ATOGEPANT Cause?

Migraine (908) Drug ineffective (581) Headache (497) Nausea (453) Constipation (376) Fatigue (282) Dizziness (192) Therapy interrupted (175) Decreased appetite (127) Therapeutic product effect incomplete (125)

What Other Drugs Cause Product use complaint?

TROFINETIDE (472) ENZALUTAMIDE (336) LIFITEGRAST (326) VOXELOTOR (298) CLASCOTERONE (285) NIRMATRELVIR\RITONAVIR (248) ABALOPARATIDE (224) ESTRADIOL (208) MOLNUPIRAVIR (206) ACETAMINOPHEN (202)

Which ATOGEPANT Alternatives Have Lower Product use complaint Risk?

ATOGEPANT vs ATOMOXETINE ATOGEPANT vs ATOMOXETINE\ATOMOXETINE ATOGEPANT vs ATORVASTATIN ATOGEPANT vs ATORVASTATIN\EZETIMIBE ATOGEPANT vs ATOSIBAN

Related Pages

ATOGEPANT Full Profile All Product use complaint Reports All Drugs Causing Product use complaint ATOGEPANT Demographics