Does PSEUDOEPHEDRINE Cause Incorrect product administration duration? 91 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 91 reports of Incorrect product administration duration have been filed in association with PSEUDOEPHEDRINE (CareOne Nasal and Sinus Decongestant). This represents 0.7% of all adverse event reports for PSEUDOEPHEDRINE.
91
Reports of Incorrect product administration duration with PSEUDOEPHEDRINE
0.7%
of all PSEUDOEPHEDRINE reports
57
Deaths
56
Hospitalizations
How Dangerous Is Incorrect product administration duration From PSEUDOEPHEDRINE?
Of the 91 reports, 57 (62.6%) resulted in death, 56 (61.5%) required hospitalization, and 56 (61.5%) 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 PSEUDOEPHEDRINE. However, 91 reports have been filed with the FAERS database.
What Other Side Effects Does PSEUDOEPHEDRINE Cause?
Drug ineffective (5,917)
Systemic lupus erythematosus (5,889)
Pain (5,790)
Pemphigus (5,726)
Rheumatoid arthritis (5,712)
Abdominal discomfort (5,654)
Alopecia (5,587)
Glossodynia (5,348)
Fatigue (5,229)
Swelling (5,184)
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)
Which PSEUDOEPHEDRINE Alternatives Have Lower Incorrect product administration duration Risk?
PSEUDOEPHEDRINE vs PSEUDOEPHEDRINE\TRIPROLIDINE
PSEUDOEPHEDRINE vs PSYLLIUM HUSK
PSEUDOEPHEDRINE vs PULMICORT FLEXHALER
PSEUDOEPHEDRINE vs PYRAZINAMIDE
PSEUDOEPHEDRINE vs PYRIDOSTIGMINE