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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ARFORMOTEROL Cause Product administration error? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product administration error have been filed in association with ARFORMOTEROL (Arformoterol Tartrate). This represents 0.5% of all adverse event reports for ARFORMOTEROL.

6
Reports of Product administration error with ARFORMOTEROL
0.5%
of all ARFORMOTEROL reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product administration error From ARFORMOTEROL?

Of the 6 reports, 1 (16.7%) required hospitalization.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ARFORMOTEROL. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does ARFORMOTEROL Cause?

Dyspnoea (242) Drug ineffective (138) Off label use (86) Malaise (73) Cough (69) Dizziness (61) Chronic obstructive pulmonary disease (59) Death (55) Headache (55) Tremor (55)

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 ARFORMOTEROL Alternatives Have Lower Product administration error Risk?

ARFORMOTEROL vs ARGATROBAN ARFORMOTEROL vs ARGININE ARFORMOTEROL vs ARGININE\LYSINE ARFORMOTEROL vs ARIMIDEX ARFORMOTEROL vs ARIPIPRAZOLE

Related Pages

ARFORMOTEROL Full Profile All Product administration error Reports All Drugs Causing Product administration error ARFORMOTEROL Demographics