FDA alerts about potential risks associated with the compounding remdesivir drug products

Feb. 10, 2021

The U.S. Food and Drug Administration (FDA) issued an alert cautioning against compounding remdesivir drug products and recommending that healthcare providers utilize the FDA-approved drug for patients who are prescribed remdesivir.

The agency reminds healthcare providers that compounded drugs are not FDA-approved and are not evaluated by FDA for safety, effectiveness or quality. Compounded drugs should only be used in patients whose medical needs cannot be met by an FDA-approved drug.

FDA approved a new drug application (NDA) for Veklury (remdesivir), a drug indicated for adults and pediatric patients (12 years of age and older and weighing at least 40 kg) for the treatment of COVID-19 requiring hospitalization on Oct. 22, 2020. The Veklury approval includes two presentations: remdesivir for injection, 100 milligrams (mg), a sterile, preservative-free lyophilized powder and remdesivir injection, 100 mg/20 milliliters (mL) (5 mg/mL), a sterile, preservative-free solution.

Veklury is an injectable drug and should only be administered in a hospital or in a healthcare setting capable of providing acute care comparable to inpatient hospital care. Important information about using Veklury to treat COVID-19 for its approved use is available in the prescribing information, which includes dosing instructions, potential side effects and drug interactions. Possible side effects include increased levels of liver enzymes, which may be a sign of liver injury; and allergic reactions, which may include changes in blood pressure and heart rate, low blood oxygen level, fever, shortness of breath, wheezing, swelling (e.g., lips, around eyes, under the skin), rash, nausea, sweating or shivering.

Complexities related to the quality and sourcing of the remdesivir active pharmaceutical ingredient (API) and formulation of remdesivir drug products may make these drugs particularly challenging to compound. Remdesivir API is complex and neither a United States Pharmacopeia (USP) monograph nor other public quality standard for the API used in FDA-approved remdesivir is available. Remdesivir API has six stereocenters and has multiple polymorphic forms. Using API forms that differ from the API in the FDA-approved drug may affect the compounded drug’s quality, including the solubility of the API in the compounded drug.

FDA is aware of various entities (separate from the suppliers named in the approved remdesivir NDA) selling what they claim to be remdesivir API. FDA often lacks detailed information about the composition and quality of the API that suppliers sell to compounders.

In addition to complexities and risks related to the API, remdesivir drug products are complex to produce. It may be challenging for compounders to formulate remdesivir drug products that will remain stable over time and have an appropriate pH. FDA-approved remdesivir is administered intravenously as an aqueous solution and remdesivir has limited aqueous solubility. FDA is concerned that compounders may have difficulty identifying an appropriate solubilizing agent and sourcing one of sufficient quality.

Moreover, the pH of the formulation in the approved drug is critical to ensure the stability of the formulation. Additionally, FDA has concerns about the compounding of remdesivir drug products with dosage forms or routes of administration that are different from the FDA-approved drug.

Because it is challenging to formulate remdesivir as a stable drug, the agency is concerned that compounded remdesivir drug products could be of low quality potentially resulting in patient harm. Furthermore, heightened interest in remdesivir due to its use in COVID-19 patients may increase the risk that a substandard or counterfeit API is sold to compounders. Given these risks, FDA is concerned about the potential for patient exposure to substandard or adulterated compounded remdesivir drug products. These concerns are further heightened because patients who are prescribed remdesivir require hospitalization and may be critically ill.

FDA cautions against compounding remdesivir drug products under section 503A of the Federal Food, Drug, and Cosmetic Act (FD&C Act).

Drug products compounded by outsourcing facilities from bulk remdesivir do not qualify for the exemptions under section 503B of the FD&C Act unless remdesivir is added to the 503B bulks list4 or the approved remdesivir product appears on FDA’s drug shortage list. If a remdesivir product is added to FDA’s drug shortage list, FDA intends to consider the applicability of policies previously communicated in guidance related to current good manufacturing practice (CGMP) requirements for outsourcing facilities given the specific quality risks associated with remdesivir API and product formulation.

The use of remdesivir API to compound drugs may potentially pose significant risks. FDA urges compounders not to compound drug products using remdesivir API and recommends that providers utilize the FDA-approved drug for patients who are prescribed remdesivir. Compounded drugs are not FDA-approved, which means FDA has not evaluated the safety, effectiveness or quality of compounded drugs. Compounded drugs should only be used in patients whose medical needs cannot be met by an FDA-approved drug.

FDA encourages consumers, patients and healthcare professionals to report adverse events or quality problems experienced with the use of compounded drugs to FDA’s MedWatch Adverse Event Reporting program:

·        Complete and submit the report online at www.fda.gov/medwatch/report.htm; or

·         Download and complete the form, then submit it via fax at 1-800-FDA-0178.

FDA has the alert.

More COVID-19 coverage HERE.

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