Does AZD-1222 Cause Incorrect product administration duration? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Incorrect product administration duration have been filed in association with AZD-1222. This represents 0.9% of all adverse event reports for AZD-1222.
20
Reports of Incorrect product administration duration with AZD-1222
0.9%
of all AZD-1222 reports
0
Deaths
19
Hospitalizations
How Dangerous Is Incorrect product administration duration From AZD-1222?
Of the 20 reports, 19 (95.0%) required hospitalization, and 1 (5.0%) 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 AZD-1222. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does AZD-1222 Cause?
Headache (838)
Fatigue (784)
Pyrexia (735)
Pain (579)
Covid-19 (515)
Arthralgia (508)
Nausea (494)
Palpitations (485)
Dyspnoea (472)
Abdominal discomfort (467)
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 AZD-1222 Alternatives Have Lower Incorrect product administration duration Risk?
AZD-1222 vs AZELAIC ACID
AZD-1222 vs AZELASTINE
AZD-1222 vs AZELASTINE\FLUTICASONE
AZD-1222 vs AZELNIDIPINE
AZD-1222 vs AZILECT