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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 Haemoptysis? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Haemoptysis have been filed in association with AZD-1222. This represents 0.3% of all adverse event reports for AZD-1222.

7
Reports of Haemoptysis with AZD-1222
0.3%
of all AZD-1222 reports
3
Deaths
1
Hospitalizations

How Dangerous Is Haemoptysis From AZD-1222?

Of the 7 reports, 3 (42.9%) resulted in death, 1 (14.3%) required hospitalization.

Is Haemoptysis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AZD-1222. However, 7 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 Haemoptysis?

RIVAROXABAN (1,961) ASPIRIN (1,255) APIXABAN (846) TREPROSTINIL (838) ALBUTEROL (652) CLOPIDOGREL BISULFATE (643) PREDNISONE (618) WARFARIN (555) ADALIMUMAB (472) TIOTROPIUM (462)

Which AZD-1222 Alternatives Have Lower Haemoptysis 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 Haemoptysis Reports All Drugs Causing Haemoptysis AZD-1222 Demographics