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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 SIROLIMUS Cause Post procedural haemorrhage? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Post procedural haemorrhage have been filed in association with SIROLIMUS (sirolimus). This represents 0.1% of all adverse event reports for SIROLIMUS.

6
Reports of Post procedural haemorrhage with SIROLIMUS
0.1%
of all SIROLIMUS reports
2
Deaths
3
Hospitalizations

How Dangerous Is Post procedural haemorrhage From SIROLIMUS?

Of the 6 reports, 2 (33.3%) resulted in death, 3 (50.0%) required hospitalization.

Is Post procedural haemorrhage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SIROLIMUS. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does SIROLIMUS Cause?

Off label use (1,960) Drug ineffective (1,005) Product use in unapproved indication (984) Transplant rejection (698) Pneumonia (599) Product use issue (506) Alopecia (491) Acne (482) Transplant dysfunction (468) Condition aggravated (433)

What Other Drugs Cause Post procedural haemorrhage?

LEVONORGESTREL (1,106) RIVAROXABAN (930) ASPIRIN (618) APIXABAN (539) ADALIMUMAB (476) IBRUTINIB (269) CLOPIDOGREL BISULFATE (235) HEPARIN (174) WARFARIN (170) DABIGATRAN ETEXILATE (121)

Which SIROLIMUS Alternatives Have Lower Post procedural haemorrhage Risk?

SIROLIMUS vs SIRUKUMAB SIROLIMUS vs SITAGLIPTIN SIROLIMUS vs SOAP SIROLIMUS vs SODIUM SIROLIMUS vs SODIUM BICARBONATE

Related Pages

SIROLIMUS Full Profile All Post procedural haemorrhage Reports All Drugs Causing Post procedural haemorrhage SIROLIMUS Demographics