Circular · Safety Notice AIFD · Güvenlik Duyuruları 07.02.2024

SB TITCK 07.02.2024 Psödoefedrin içeren İlaçlar Acil Güvenlilik Kısıtlaması Görüş Katkı

EN: This is the official English version published by the authority (TİTCK), imported from the AIFD Legislation Portal archive. The binding text is the official Turkish version.

SB TITCK 07.02.2024 Psödoefedrin içeren İlaçlar Acil Güvenlilik Kısıtlaması Görüş Katkı_EN

Turkish Ministry of Health Turkish Medicines and Medical Devices Agency

Number: E-24931227-510.01.04-1377975 07.02.2024 Subject: Pseudoephedrine-containing products /
Urgent Safety Restriction / Request for Opinions and Suggestions

FILE

The Agency has given consideration to the warnings recommended by the Pharmacovigilance Risk Assessment Committee (PRAC), and approved by the Committee for Medicinal Products for Human Use (CHMP) of European Medicines Agency (EMA), regarding pseudoephedrine-containing drugs (both for single and combination use) to mitigate the risk of posterior reversible encephalopathy syndrome (PRES) and reversible cerebral vasoconstriction syndrome (RCVS). Accordingly, the statements described in the attachment must be incorporated in local summary of product characteristics (KÜP) and package leaflet (KT) of the products concerned.
Please forward any opinions, views and suggestions regarding the foregoing to the Pharmacovigilance Risk Management Unit at the Pharmacovigilance and Controlled Substances Department by 19.02.2024, and refrain from making any submissions to the Pharmacologic Assessment Unit in the mean time.
For your information and appropriate action.

Dr. Asım Hocaoğlu Agency President

Distribution: Turkish Pharmaceutical Manufacturers’ Association
Association of Research-Based Pharmaceutical Companies
Pharmaceutical Manufacturers’ Association of Türkiye
Health Products Association

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Turkish Ministry of Health Turkish Medicines and Medical Devices Agency

[Product information of all products must be revised as follows (add, revise or delete text as appropriate)]

Local Summary of Product Characteristics (KÜB)

4.3 Contraindications
[Incorporate the following contraindications]

Severe hypertension or uncontrolled hypertension Severe acute or chronic kidney disease/renal failure

4.4 Special warnings and precautions for use [Incorporate the following warning]

Posterior reversible encephalopathy syndrome (PRES) and reversible cerebral vasoconstriction syndrome (RCVS)

Cases of PRES and RCVS have been reported with the use of pseudoephedrine-containing products (see section 4.8). The risk is increased in patients with severe or uncontrolled hypertension, or with severe acute or chronic kidney disease/renal failure (see section 4.3).

Pseudoephedrine should be discontinued and immediate medical assistance sought if the following symptoms occur: sudden severe headache or thunderclap headache, nausea, vomiting, confusion, seizures and/or visual disturbances. Most reported cases of PRES and RCVS resolved following discontinuation and appropriate treatment.

4.8 Undesirable effects [Revise as appropriate or incorporate the following adverse reactions in System Organ Class, under the section “Nervous system disorders” with a frequency of “Unknown”]

Posterior reversible encephalopathy syndrome (PRES) (see Section 4.4) Reversible cerebral vasoconstriction syndrome (RCVS) (see Section 4.4)

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Turkish Ministry of Health Turkish Medicines and Medical Devices Agency

Local Package Leaflet (KT)

  1. What you need to know before you take [Incorporate the following]

DO NOT TAKE in the following cases:

Very high blood pressure (severe hypertension) or hypertension not controlled by your medication Severe acute (sudden) or chronic (long-term) kidney disease or kidney failure.

EXERCISE CAUTION when using in the following cases: Cases of posterior reversible encephalopathy syndrome (PRES) and reversible cerebral vasoconstriction syndrome (RCVS) have been reported following use of medicines containing pseudoephedrine. PRES and RCVS are rare conditions that can involve reduced blood supply to the brain. Stop using immediately and seek immediate medical assistance if you develop symptoms that may be signs of PRES or RCVS (see section 4 “Possible side effects” for symptoms).

  1. Possible side effects [The most serious side effect below should be listed first in section 4]

Not known: Frequency cannot be estimated from the available data

Serious conditions affecting blood vessels in the brain known as posterior reversible encephalopathy syndrome (PRES) and reversible cerebral vasoconstriction syndrome (RCVS)

Stop using immediately and seek urgent medical assistance if you develop the following symptoms which may be signs of posterior reversible encephalopathy syndrome (PRES) or reversible cerebral vasoconstriction syndrome (RCVS):

Severe headache with a sudden onset Feeling sick Vomiting Confusion Seizures, changes in vision

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