Does ATOGEPANT Cause Wrong technique in product usage process? 45 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Wrong technique in product usage process have been filed in association with ATOGEPANT (Qulipta). This represents 1.0% of all adverse event reports for ATOGEPANT.
45
Reports of Wrong technique in product usage process with ATOGEPANT
1.0%
of all ATOGEPANT reports
0
Deaths
2
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ATOGEPANT?
Of the 45 reports, 2 (4.4%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ATOGEPANT. However, 45 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ATOGEPANT Alternatives Have Lower Wrong technique in product usage process Risk?
ATOGEPANT vs ATOMOXETINE
ATOGEPANT vs ATOMOXETINE\ATOMOXETINE
ATOGEPANT vs ATORVASTATIN
ATOGEPANT vs ATORVASTATIN\EZETIMIBE
ATOGEPANT vs ATOSIBAN