Does UNSPECIFIED INGREDIENT Cause International normalised ratio increased? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of International normalised ratio increased have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.1% of all adverse event reports for UNSPECIFIED INGREDIENT.
28
Reports of International normalised ratio increased with UNSPECIFIED INGREDIENT
0.1%
of all UNSPECIFIED INGREDIENT reports
2
Deaths
20
Hospitalizations
How Dangerous Is International normalised ratio increased From UNSPECIFIED INGREDIENT?
Of the 28 reports, 2 (7.1%) resulted in death, 20 (71.4%) required hospitalization, and 2 (7.1%) were considered life-threatening.
Is International normalised ratio increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 28 reports have been filed with the FAERS database.
What Other Side Effects Does UNSPECIFIED INGREDIENT Cause?
Death (2,090)
Off label use (1,306)
Drug ineffective (1,227)
Completed suicide (1,190)
Nausea (1,041)
Fatigue (1,020)
Dyspnoea (934)
Pneumonia (903)
Asthenia (894)
Vomiting (877)
What Other Drugs Cause International normalised ratio increased?
WARFARIN (5,622)
RIVAROXABAN (863)
ACETAMINOPHEN (533)
ASPIRIN (448)
APIXABAN (317)
CLOPIDOGREL BISULFATE (314)
FLUINDIONE (286)
AMIODARONE (277)
FUROSEMIDE (277)
DABIGATRAN ETEXILATE (223)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower International normalised ratio increased Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN