MHRA Recalls Sertraline Batch After Citalopram Mix-Up, Urges Patients to Check Packs
Sertraline Recall: Check Packs for Wrong Drug, MHRA Warns

Millions of patients taking antidepressants are being urged to check their tablets after a manufacturing error led to two drugs being incorrectly packaged. The Medicines and Healthcare products Regulatory Agency (MHRA) has issued a warning that packs of Sertraline may contain blister strips of Citalopram inside the sealed packet.

Both drugs are selective serotonin reuptake inhibitors (SSRIs), commonly prescribed to treat depression, anxiety, and other mood disorders by boosting serotonin levels in the brain. However, accidentally taking the wrong medication can have serious side effects, the MHRA warns, requiring urgent medical attention.

Precautionary Recall Issued

Officials have now issued a precautionary recall for one batch of Sertraline 100mg film-coated tablets with batch number V2500425. Patients prescribed this medication are urged to check their boxes contain the correct drug, ensuring that the blister strips match the batch number and expiry date printed on the outer packaging.

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"If the blister strips inside the carton are labelled Citalopram 40mg, please contact your pharmacy as soon as possible," said Dr. Alison Cave, MHRA Chief Safety Officer. "Patients who have accidentally taken Citalopram instead of, or as well as, Sertraline may experience heightened serotonergic side effects. These can include nausea, headache, sleep changes, and mild anxiety."

What Patients Should Do

Patients who have been correctly prescribed Sertraline 100mg do not need to take further action. However, anyone who finds their medication is incorrect should return the pack to their pharmacy for a replacement.

The MHRA advises that anyone experiencing severe symptoms after taking the wrong medication should seek medical help immediately. The agency is working with manufacturers to rectify the issue and prevent further errors.

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