Does AZD-1222 Cause Activated partial thromboplastin time prolonged? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Activated partial thromboplastin time prolonged have been filed in association with AZD-1222. This represents 0.6% of all adverse event reports for AZD-1222.
14
Reports of Activated partial thromboplastin time prolonged with AZD-1222
0.6%
of all AZD-1222 reports
4
Deaths
4
Hospitalizations
How Dangerous Is Activated partial thromboplastin time prolonged From AZD-1222?
Of the 14 reports, 4 (28.6%) resulted in death, 4 (28.6%) required hospitalization, and 6 (42.9%) were considered life-threatening.
Is Activated partial thromboplastin time prolonged Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZD-1222. However, 14 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 Activated partial thromboplastin time prolonged?
DABIGATRAN ETEXILATE (264)
HEPARIN (225)
RIVAROXABAN (163)
WARFARIN (146)
ACETAMINOPHEN (119)
ALLOPURINOL (110)
AMIODARONE (99)
METRONIDAZOLE (98)
SIMVASTATIN (94)
DARBEPOETIN ALFA (93)
Which AZD-1222 Alternatives Have Lower Activated partial thromboplastin time prolonged Risk?
AZD-1222 vs AZELAIC ACID
AZD-1222 vs AZELASTINE
AZD-1222 vs AZELASTINE\FLUTICASONE
AZD-1222 vs AZELNIDIPINE
AZD-1222 vs AZILECT