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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 ZINNAT Cause Post procedural haemorrhage? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Post procedural haemorrhage have been filed in association with ZINNAT. This represents 17.7% of all adverse event reports for ZINNAT.

9
Reports of Post procedural haemorrhage with ZINNAT
17.7%
of all ZINNAT reports
0
Deaths
9
Hospitalizations

How Dangerous Is Post procedural haemorrhage From ZINNAT?

Of the 9 reports, 9 (100.0%) 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 ZINNAT. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does ZINNAT Cause?

Dyspnoea (7) Poor quality drug administered (5) Product contamination physical (5) Product deposit (5) Toxic anterior segment syndrome (5)

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)

Related Pages

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