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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 RALTEGRAVIR Cause Maternal exposure timing unspecified? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Maternal exposure timing unspecified have been filed in association with RALTEGRAVIR (ISENTRESS). This represents 0.1% of all adverse event reports for RALTEGRAVIR.

6
Reports of Maternal exposure timing unspecified with RALTEGRAVIR
0.1%
of all RALTEGRAVIR reports
1
Deaths
0
Hospitalizations

How Dangerous Is Maternal exposure timing unspecified From RALTEGRAVIR?

Of the 6 reports, 1 (16.7%) resulted in death.

Is Maternal exposure timing unspecified Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RALTEGRAVIR. However, 6 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 Maternal exposure timing unspecified?

RITUXIMAB (402) METHOTREXATE (350) ADALIMUMAB (343) DICLOFENAC (331) TOCILIZUMAB (327) HYDROXYCHLOROQUINE (309) FOLIC ACID (304) INFLIXIMAB (303) LEFLUNOMIDE (302) SECUKINUMAB (301)

Which RALTEGRAVIR Alternatives Have Lower Maternal exposure timing unspecified Risk?

RALTEGRAVIR vs RALTITREXED RALTEGRAVIR vs RAMELTEON RALTEGRAVIR vs RAMIPRIL RALTEGRAVIR vs RAMUCIRUMAB RALTEGRAVIR vs RANEXA

Related Pages

RALTEGRAVIR Full Profile All Maternal exposure timing unspecified Reports All Drugs Causing Maternal exposure timing unspecified RALTEGRAVIR Demographics