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Update on Rifamycin Issues

September 14, 2020

Dear Colleague:

On August 26, 2020, FDA issued a statementexternal icon related to mitigating shortages of rifampin and rifapentine and its interim guidance to continue using these drugs in the treatment of tuberculosis (TB) after nitrosamine-class impurities were detected through recently adopted regulatory standards to assay all medications for nitrosamines.  FDA sets standard limits on the concentrations of the impurities and is allowing distribution of rifampin and rifapentine if the concentrations do not exceed interim limits while the impurities are investigated. This letter updates CDC’s Division of TB Elimination (DTBE) Dear Colleague Letters of June 19 and August 19, 2020. CDC’s DTBE recommends that providers continue prescribing rifampin and rifapentine for all TB and latent TB infection (LTBI) treatment per existing guidelines.

Background

FDA only recently began including testing for nitrosamines, which are potential carcinogens, in rifampin and rifapentine as part of its drug safety requirements. It is possible that nitrosamines were present in rifampin and rifapentine for a substantial time (years or decades) prior to introduction of these tests. DTBE is not aware of any data showing an association between cancer and use of rifamycins in humans. However, DTBE is also not aware of any rigorous studies that have looked for this association.

Information on Rifampin

Unrelated to the detection of nitrosamine impurities, Sanofi announced the discontinuation of three oral rifampin-containing products: Rifadin® (rifampin 150 mg and 300 mg capsules); Rifamate® (a fixed-drug combination of isoniazid and rifampin), and Rifater® (a fixed-drug combination of isoniazid, rifampin, and pyrazinamide) in June 2020.  Information on drug shortages and discontinuations is available from FDAexternal icon.  FDA is working with other manufacturers to maintain availability of rifampin, and there is no national shortage of rifampin at present. Rifampin should be prescribed as an essential part of a multi-drug regimen for the treatment of active TB diseaseexternal icon. Rifampin can also be prescribed, as 3 months of daily isoniazid and rifampin (3HR) or 4 months of daily rifampin (4R), for treating LTBI to prevent the development of active TB disease per current National TB Controllers Association (NTCA)/CDC guidelines.

Information on Rifapentine

In June 2020, shipments of rifapentine (supplied as Priftin® 150 mg film-coated tablets manufactured by Sanofi) were paused after a nitrosamine impurity was found. FDA and Sanofi have not announced when shipments will resume, and FDAexternal icon still lists rifapentine as “Currently in Shortage.” Where local supplies of rifapentine are enough for complete regimens, providers can continue to prescribe the 3-month regimen of weekly rifapentine with isoniazid (3HP) for treating LTBI. Where rifapentineexternal icon is in shortage, providers can consider other rifamycin-based regimens such as 3HR or 4R, which have completion rates comparable to 3HP.

Information on Drug Treatment Continuation for LTBI

Patients who are already taking rifampin or rifapentine-containing regimens for LTBI can continue their treatment. If a clinician or a patient prefers to discontinue one of these regimens, a complete regimen of 6 or 9 months of isoniazid can be started, or the original regimen can be completed with a proportionate duration of one of the isoniazid-only regimens. However, isoniazid regimens are associated with increased risk of drug-induced liver injury and lower completion rates. Therefore, CDC does not recommend discontinuing rifamycin-based short-course LTBI treatment in favor of isoniazid-only treatment unless necessitated by another event (e.g., adverse reaction to a rifamycin).

Reporting Rifamycin Supply Issues

Information of drug shortages and discontinuations are available from FDAexternal icon. DTBE recommends that you periodically assess your rifampin and rifapentine availability with your pharmacy or your suppliers. Please keep your CDC project officer for your jurisdiction’s TB cooperative agreement updated by e-mail message or telephone. If you find a shortage or if you are forecasting a shortage, please notify FDA directly by e-mail (drugshortages@fda.hhs.gov) or telephone (240-402-7770). You also can report a shortage to the National Tuberculosis Controllers Association (NTCA) with a form on its home page, http://www.tbcontrollers.org/external icon. Questions related to this letter should be sent to CDC by email (tbinfo@cdc.gov) or phone (770-488-7100).

CDC will continue to monitor the situation closely and work with our partners at FDAexternal icon, NTCAexternal icon, state and local health departments, and the TB Centers of Excellence for Training, Education, and Medical Consultation to ensure TB patients continue to receive safe and effective treatment.

Sincerely,

Terry Chorba
Terence Chorba, MD, DSc
Chief, Field Services Branch, Division of Tuberculosis Elimination
National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention
Centers for Disease Control and Prevention
1600 Clifton Road NE (US 12-4), Atlanta, GA 30329

 

 

Page last reviewed: September 14, 2020