Does ATOMOXETINE Cause Incorrect product administration duration? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Incorrect product administration duration have been filed in association with ATOMOXETINE (Atomoxetine). This represents 0.3% of all adverse event reports for ATOMOXETINE.
31
Reports of Incorrect product administration duration with ATOMOXETINE
0.3%
of all ATOMOXETINE reports
29
Deaths
29
Hospitalizations
How Dangerous Is Incorrect product administration duration From ATOMOXETINE?
Of the 31 reports, 29 (93.5%) resulted in death, 29 (93.5%) required hospitalization, and 29 (93.5%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ATOMOXETINE. However, 31 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which ATOMOXETINE Alternatives Have Lower Incorrect product administration duration Risk?
ATOMOXETINE vs ATOMOXETINE\ATOMOXETINE
ATOMOXETINE vs ATORVASTATIN
ATOMOXETINE vs ATORVASTATIN\EZETIMIBE
ATOMOXETINE vs ATOSIBAN
ATOMOXETINE vs ATOVAQUONE