Does IPRATROPIUM\IPRATROPIUM ANHYDROUS Cause Device issue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device issue have been filed in association with IPRATROPIUM\IPRATROPIUM ANHYDROUS. This represents 1.2% of all adverse event reports for IPRATROPIUM\IPRATROPIUM ANHYDROUS.
5
Reports of Device issue with IPRATROPIUM\IPRATROPIUM ANHYDROUS
1.2%
of all IPRATROPIUM\IPRATROPIUM ANHYDROUS reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device issue From IPRATROPIUM\IPRATROPIUM ANHYDROUS?
Of the 5 reports.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IPRATROPIUM\IPRATROPIUM ANHYDROUS. However, 5 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which IPRATROPIUM\IPRATROPIUM ANHYDROUS Alternatives Have Lower Device issue 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