Does IPRATROPIUM Cause Product administration error? 38 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Product administration error have been filed in association with IPRATROPIUM (Ipratropium bromide). This represents 0.5% of all adverse event reports for IPRATROPIUM.
38
Reports of Product administration error with IPRATROPIUM
0.5%
of all IPRATROPIUM reports
4
Deaths
32
Hospitalizations
How Dangerous Is Product administration error From IPRATROPIUM?
Of the 38 reports, 4 (10.5%) resulted in death, 32 (84.2%) required hospitalization, and 5 (13.2%) 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 IPRATROPIUM. However, 38 reports have been filed with the FAERS database.
What Other Side Effects Does IPRATROPIUM Cause?
Asthma (2,596)
Dyspnoea (2,450)
Wheezing (1,910)
Cough (1,315)
Therapeutic product effect incomplete (1,229)
Obstructive airways disorder (1,171)
Drug ineffective (1,057)
Pneumonia (931)
Loss of personal independence in daily activities (861)
Chest discomfort (785)
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 IPRATROPIUM Alternatives Have Lower Product administration error Risk?
IPRATROPIUM vs IPRATROPIUM\IPRATROPIUM ANHYDROUS
IPRATROPIUM vs IPTACOPAN
IPRATROPIUM vs IRBESARTAN
IPRATROPIUM vs IRINOTECAN
IPRATROPIUM vs IRON