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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 TICAGRELOR Cause Product administration error? 15 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Product administration error have been filed in association with TICAGRELOR (Ticagrelor). This represents 0.1% of all adverse event reports for TICAGRELOR.

15
Reports of Product administration error with TICAGRELOR
0.1%
of all TICAGRELOR reports
1
Deaths
10
Hospitalizations

How Dangerous Is Product administration error From TICAGRELOR?

Of the 15 reports, 1 (6.7%) resulted in death, 10 (66.7%) required hospitalization.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TICAGRELOR. However, 15 reports have been filed with the FAERS database.

What Other Side Effects Does TICAGRELOR Cause?

Dyspnoea (3,156) Myocardial infarction (1,749) Death (1,510) Off label use (1,084) Fatigue (1,081) Chest pain (1,075) Contusion (970) Dizziness (811) Vascular stent thrombosis (700) Haemorrhage (676)

What Other Drugs Cause Product administration error?

HYDROXYPROGESTERONE CAPROATE (972) ACETAMINOPHEN (666) CENEGERMIN-BKBJ (613) LEUPROLIDE (595) EVOLOCUMAB (565) ADALIMUMAB (543) METHYLPHENIDATE (414) OLMESARTAN MEDOXOMIL (314) ASPIRIN (241) SECUKINUMAB (225)

Which TICAGRELOR Alternatives Have Lower Product administration error Risk?

TICAGRELOR vs TICLOPIDINE TICAGRELOR vs TIGECYCLINE TICAGRELOR vs TIKOSYN TICAGRELOR vs TILDRAKIZUMAB TICAGRELOR vs TILDRAKIZUMAB-ASMN

Related Pages

TICAGRELOR Full Profile All Product administration error Reports All Drugs Causing Product administration error TICAGRELOR Demographics