Does CAFFEINE\CHLORPHENIRAMINE\PHENYLPROPANOLAMINE Cause Incorrect product administration duration? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Incorrect product administration duration have been filed in association with CAFFEINE\CHLORPHENIRAMINE\PHENYLPROPANOLAMINE. This represents 5.7% of all adverse event reports for CAFFEINE\CHLORPHENIRAMINE\PHENYLPROPANOLAMINE.
5
Reports of Incorrect product administration duration with CAFFEINE\CHLORPHENIRAMINE\PHENYLPROPANOLAMINE
5.7%
of all CAFFEINE\CHLORPHENIRAMINE\PHENYLPROPANOLAMINE reports
5
Deaths
5
Hospitalizations
How Dangerous Is Incorrect product administration duration From CAFFEINE\CHLORPHENIRAMINE\PHENYLPROPANOLAMINE?
Of the 5 reports, 5 (100.0%) resulted in death, 5 (100.0%) required hospitalization, and 5 (100.0%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CAFFEINE\CHLORPHENIRAMINE\PHENYLPROPANOLAMINE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does CAFFEINE\CHLORPHENIRAMINE\PHENYLPROPANOLAMINE Cause?
Pericarditis (70)
Pemphigus (65)
Helicobacter infection (63)
Irritable bowel syndrome (63)
Lower respiratory tract infection (62)
Peripheral swelling (61)
Duodenal ulcer perforation (60)
Impaired healing (60)
Hypersensitivity (59)
Joint swelling (59)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)