Does FORMOTEROL\MOMETASONE Cause Product administration error? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration error have been filed in association with FORMOTEROL\MOMETASONE. This represents 1.2% of all adverse event reports for FORMOTEROL\MOMETASONE.
5
Reports of Product administration error with FORMOTEROL\MOMETASONE
1.2%
of all FORMOTEROL\MOMETASONE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product administration error From FORMOTEROL\MOMETASONE?
Of the 5 reports, 5 (100.0%) 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 FORMOTEROL\MOMETASONE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does FORMOTEROL\MOMETASONE Cause?
Asthma (356)
Dyspnoea (282)
Wheezing (253)
Therapeutic product effect incomplete (240)
Cough (160)
Loss of personal independence in daily activities (122)
Sleep disorder due to a general medical condition (122)
Condition aggravated (106)
Obstructive airways disorder (106)
Full blood count abnormal (100)
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\MOMETASONE Alternatives Have Lower Product administration error Risk?
FORMOTEROL\MOMETASONE vs FORMOTEROL\MOMETASONE FUROATE
FORMOTEROL\MOMETASONE vs FORTEO
FORMOTEROL\MOMETASONE vs FOSAMAX
FORMOTEROL\MOMETASONE vs FOSAMPRENAVIR
FORMOTEROL\MOMETASONE vs FOSAPREPITANT