Does MOMETASONE 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 MOMETASONE (MOMETASONE FUROATE). This represents 0.4% of all adverse event reports for MOMETASONE.
7
Reports of Product administration error with MOMETASONE
0.4%
of all MOMETASONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From MOMETASONE?
Of the 7 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MOMETASONE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does MOMETASONE Cause?
Asthma (522)
Dyspnoea (497)
Wheezing (459)
Gastrooesophageal reflux disease (406)
Therapeutic product effect incomplete (400)
Drug ineffective (318)
Sleep disorder due to a general medical condition (318)
Cardiac disorder (311)
Headache (308)
Loss of personal independence in daily activities (301)
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 MOMETASONE Alternatives Have Lower Product administration error Risk?
MOMETASONE vs MOMETASONE FUROATE
MOMETASONE vs MOMETASONE FUROATE\OLOPATADINE
MOMETASONE vs MONOMETHYL
MOMETASONE vs MONTELUKAST
MOMETASONE vs MONTELUKAST\MONTELUKAST