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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does AZD-1222 Cause Drug hypersensitivity? 17 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Drug hypersensitivity have been filed in association with AZD-1222. This represents 0.7% of all adverse event reports for AZD-1222.

17
Reports of Drug hypersensitivity with AZD-1222
0.7%
of all AZD-1222 reports
0
Deaths
13
Hospitalizations

How Dangerous Is Drug hypersensitivity From AZD-1222?

Of the 17 reports, 13 (76.5%) required hospitalization.

Is Drug hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AZD-1222. However, 17 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 Drug hypersensitivity?

METHOTREXATE (16,677) ETANERCEPT (12,991) ADALIMUMAB (11,599) MORPHINE (11,095) RITUXIMAB (8,924) LEFLUNOMIDE (8,148) INFLIXIMAB (8,119) TOCILIZUMAB (7,883) ABATACEPT (7,808) CODEINE (7,479)

Which AZD-1222 Alternatives Have Lower Drug hypersensitivity Risk?

AZD-1222 vs AZELAIC ACID AZD-1222 vs AZELASTINE AZD-1222 vs AZELASTINE\FLUTICASONE AZD-1222 vs AZELNIDIPINE AZD-1222 vs AZILECT

Related Pages

AZD-1222 Full Profile All Drug hypersensitivity Reports All Drugs Causing Drug hypersensitivity AZD-1222 Demographics