Remdesivir — Active Pharmaceutical Ingredient

Remdesivir is an active pharmaceutical ingredient found in 1 FDA-approved drug product. Forms: SOLUTION, POWDER. Routes: INTRAVENOUS.

This content is for informational purposes only. Always consult a healthcare professional.

Remdesivir (1 brand name, 2 dosage forms, 1 route)

Available dosage forms: SOLUTION, POWDER.

Routes of administration: INTRAVENOUS.

Brand Names

  • VEKLURY

Indications and Usage

VEKLURY is indicated for the treatment of coronavirus disease 2019 (COVID-19) in adults and pediatric patients (birth to less than 18 years of age weighing at least 1.5 kg) who are [see Clinical Studies (14)]: Hospitalized, or Not hospitalized and have mild-to-moderate COVID-19, and are at high risk for progression to severe COVID-19, including hospitalization or death.

Contraindications

VEKLURY is contraindicated in patients with a history of clinically significant hypersensitivity reactions to VEKLURY or any components of the product [see Warnings and Precautions (5.1)].

Adverse Reactions

The following adverse reactions are discussed in other sections of the labeling: Hypersensitivity Including Infusion-related and Anaphylactic Reactions [see Warnings and Precautions (5.1)] Increased Risk of Transaminase Elevations [see Warnings and Precautions (5.2)]

Mechanism of Action

Remdesivir is an antiviral drug with activity against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) [see Microbiology (12.4)].

Overdosage

There is no human experience of acute overdosage with VEKLURY. Treatment of overdose with VEKLURY should consist of general supportive measures including monitoring of vital signs and observation of the clinical status of the patient. There is no specific antidote for overdose with VEKLURY.

⚠ Caution
Medical Disclaimer: This information is for educational purposes only. Always consult a healthcare professional before taking any medication.