Does ATOMOXETINE Cause Product quality issue? 407 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 407 reports of Product quality issue have been filed in association with ATOMOXETINE (Atomoxetine). This represents 4.4% of all adverse event reports for ATOMOXETINE.
407
Reports of Product quality issue with ATOMOXETINE
4.4%
of all ATOMOXETINE reports
389
Deaths
342
Hospitalizations
How Dangerous Is Product quality issue From ATOMOXETINE?
Of the 407 reports, 389 (95.6%) resulted in death, 342 (84.0%) required hospitalization, and 350 (86.0%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ATOMOXETINE. However, 407 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 Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which ATOMOXETINE Alternatives Have Lower Product quality issue Risk?
ATOMOXETINE vs ATOMOXETINE\ATOMOXETINE
ATOMOXETINE vs ATORVASTATIN
ATOMOXETINE vs ATORVASTATIN\EZETIMIBE
ATOMOXETINE vs ATOSIBAN
ATOMOXETINE vs ATOVAQUONE