Does RALTEGRAVIR Cause International normalised ratio increased? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of International normalised ratio increased have been filed in association with RALTEGRAVIR (ISENTRESS). This represents 0.1% of all adverse event reports for RALTEGRAVIR.
5
Reports of International normalised ratio increased with RALTEGRAVIR
0.1%
of all RALTEGRAVIR reports
4
Deaths
4
Hospitalizations
How Dangerous Is International normalised ratio increased From RALTEGRAVIR?
Of the 5 reports, 4 (80.0%) resulted in death, 4 (80.0%) required hospitalization, and 4 (80.0%) 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 RALTEGRAVIR. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does RALTEGRAVIR Cause?
Foetal exposure during pregnancy (1,033)
Maternal exposure during pregnancy (726)
Exposure during pregnancy (700)
Drug interaction (552)
Virologic failure (517)
Depression (482)
Death (431)
Pathogen resistance (425)
Drug resistance (388)
No adverse event (339)
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 RALTEGRAVIR Alternatives Have Lower International normalised ratio increased Risk?
RALTEGRAVIR vs RALTITREXED
RALTEGRAVIR vs RAMELTEON
RALTEGRAVIR vs RAMIPRIL
RALTEGRAVIR vs RAMUCIRUMAB
RALTEGRAVIR vs RANEXA