Does ATOMOXETINE Cause Maternal exposure timing unspecified? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Maternal exposure timing unspecified have been filed in association with ATOMOXETINE (Atomoxetine). This represents 0.3% of all adverse event reports for ATOMOXETINE.
29
Reports of Maternal exposure timing unspecified with ATOMOXETINE
0.3%
of all ATOMOXETINE reports
29
Deaths
29
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From ATOMOXETINE?
Of the 29 reports, 29 (100.0%) resulted in death, 29 (100.0%) required hospitalization, and 29 (100.0%) were considered life-threatening.
Is Maternal exposure timing unspecified Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ATOMOXETINE. However, 29 reports have been filed with the FAERS database.
What Other Side Effects Does ATOMOXETINE Cause?
Drug ineffective (1,352)
Off label use (1,132)
Nausea (889)
Vomiting (820)
Fatigue (786)
Abdominal pain upper (755)
Headache (741)
Dizziness (720)
Pain (705)
Insomnia (695)
What Other Drugs Cause Maternal exposure timing unspecified?
RITUXIMAB (402)
METHOTREXATE (350)
ADALIMUMAB (343)
DICLOFENAC (331)
TOCILIZUMAB (327)
HYDROXYCHLOROQUINE (309)
FOLIC ACID (304)
INFLIXIMAB (303)
LEFLUNOMIDE (302)
SECUKINUMAB (301)
Which ATOMOXETINE Alternatives Have Lower Maternal exposure timing unspecified Risk?
ATOMOXETINE vs ATOMOXETINE\ATOMOXETINE
ATOMOXETINE vs ATORVASTATIN
ATOMOXETINE vs ATORVASTATIN\EZETIMIBE
ATOMOXETINE vs ATOSIBAN
ATOMOXETINE vs ATOVAQUONE