Does IPRATROPIUM\IPRATROPIUM ANHYDROUS Cause Device defective? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Device defective have been filed in association with IPRATROPIUM\IPRATROPIUM ANHYDROUS. This represents 3.8% of all adverse event reports for IPRATROPIUM\IPRATROPIUM ANHYDROUS.
16
Reports of Device defective with IPRATROPIUM\IPRATROPIUM ANHYDROUS
3.8%
of all IPRATROPIUM\IPRATROPIUM ANHYDROUS reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device defective From IPRATROPIUM\IPRATROPIUM ANHYDROUS?
Of the 16 reports.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IPRATROPIUM\IPRATROPIUM ANHYDROUS. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does IPRATROPIUM\IPRATROPIUM ANHYDROUS Cause?
Product delivery mechanism issue (105)
Dyspnoea (77)
Off label use (69)
Product dose omission issue (69)
Condition aggravated (62)
Vomiting (61)
Abdominal distension (59)
Nausea (56)
Drug ineffective (54)
No adverse event (54)
What Other Drugs Cause Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which IPRATROPIUM\IPRATROPIUM ANHYDROUS Alternatives Have Lower Device defective Risk?
IPRATROPIUM\IPRATROPIUM ANHYDROUS vs IPTACOPAN
IPRATROPIUM\IPRATROPIUM ANHYDROUS vs IRBESARTAN
IPRATROPIUM\IPRATROPIUM ANHYDROUS vs IRINOTECAN
IPRATROPIUM\IPRATROPIUM ANHYDROUS vs IRON
IPRATROPIUM\IPRATROPIUM ANHYDROUS vs IRON DEXTRAN