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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 Haemoglobin increased? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Haemoglobin increased have been filed in association with AZD-1222. This represents 0.2% of all adverse event reports for AZD-1222.

5
Reports of Haemoglobin increased with AZD-1222
0.2%
of all AZD-1222 reports
0
Deaths
5
Hospitalizations

How Dangerous Is Haemoglobin increased From AZD-1222?

Of the 5 reports, 5 (100.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.

Is Haemoglobin increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AZD-1222. However, 5 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 Haemoglobin increased?

RUXOLITINIB (332) TREPROSTINIL (245) SOTATERCEPT (151) CLOZAPINE (142) SOTATERCEPT-CSRK (100) DARBEPOETIN ALFA (99) TESTOSTERONE (96) METFORMIN (93) VOXELOTOR (86) ROSUVASTATIN (85)

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