Freedom of Information request on penfluridol licensing in the UK (FOI 21-539)
Published 13 August 2021
14th June 2021 FOI 21/539
Dear
Thank you for your email.
According to our records we confirm this product is not licensed in the UK and as such we do not hold this information.
Whilst penfluridol is not licensed for use in the UK, we can confirm to up to and including 6th June 2021 we have received 1 Adverse Drug Reaction (ADR) report in association with penfluridol reporting ‘Increased viscosity of upper respiratory secretion’. Reporting of a particular reaction does not necessarily mean that it has been caused by the drug, only that the reporter has a suspicion it may have. Underlying or concurrent illnesses may be responsible and such events can also be coincidental.
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Yours sincerely,
MHRA Customer Service Centre
Medicines and Healthcare products Regulatory Agency 10 South Colonnade, Canary Wharf, London E14 4PU