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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 RAMIPRIL Cause Maternal exposure timing unspecified? 94 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 94 reports of Maternal exposure timing unspecified have been filed in association with RAMIPRIL (Ramipril). This represents 0.3% of all adverse event reports for RAMIPRIL.

94
Reports of Maternal exposure timing unspecified with RAMIPRIL
0.3%
of all RAMIPRIL reports
90
Deaths
93
Hospitalizations

How Dangerous Is Maternal exposure timing unspecified From RAMIPRIL?

Of the 94 reports, 90 (95.7%) resulted in death, 93 (98.9%) required hospitalization, and 92 (97.9%) were considered life-threatening.

Is Maternal exposure timing unspecified Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RAMIPRIL. However, 94 reports have been filed with the FAERS database.

What Other Side Effects Does RAMIPRIL Cause?

Acute kidney injury (3,286) Dyspnoea (2,537) Dizziness (2,490) Hypotension (2,417) Fatigue (2,415) Drug ineffective (2,412) Nausea (2,219) Vomiting (2,055) Off label use (2,053) Hypertension (2,046)

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 RAMIPRIL Alternatives Have Lower Maternal exposure timing unspecified Risk?

RAMIPRIL vs RAMUCIRUMAB RAMIPRIL vs RANEXA RAMIPRIL vs RANIBIZUMAB RAMIPRIL vs RANIMUSTINE RAMIPRIL vs RANITIDINE

Related Pages

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