Does FORMOTEROL Cause Product administration error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product administration error have been filed in association with FORMOTEROL (Formoterol fumarate). This represents 0.3% of all adverse event reports for FORMOTEROL.
7
Reports of Product administration error with FORMOTEROL
0.3%
of all FORMOTEROL reports
3
Deaths
3
Hospitalizations
How Dangerous Is Product administration error From FORMOTEROL?
Of the 7 reports, 3 (42.9%) resulted in death, 3 (42.9%) required hospitalization, and 2 (28.6%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FORMOTEROL. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does FORMOTEROL Cause?
Asthma (1,204)
Dyspnoea (1,090)
Wheezing (632)
Cough (553)
Obstructive airways disorder (504)
Therapeutic product effect incomplete (467)
Drug ineffective (456)
Gastrooesophageal reflux disease (434)
Full blood count abnormal (344)
Loss of personal independence in daily activities (307)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which FORMOTEROL Alternatives Have Lower Product administration error Risk?
FORMOTEROL vs FORMOTEROL\GLYCOPYRROLATE
FORMOTEROL vs FORMOTEROL\MOMETASONE
FORMOTEROL vs FORMOTEROL\MOMETASONE FUROATE
FORMOTEROL vs FORTEO
FORMOTEROL vs FOSAMAX