Citalopram
Brand names: Cipramil
Citalopram is a selective serotonin reuptake inhibitor (SSRI) used for depression and panic disorder.
Adult dose
Dose adjustments
Dosage adjustment is not necessary in cases of mild or moderate renal impairment. No information is available in cases of severe renal impairment (creatinine clearance <20 mL/min) (§4.2).
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
US labelling (FDA)
Reference — US labelling, may differ from UKAdminister once daily with or without food ( 2 ) . Initial dosage is 20 mg once daily; after one week may increase to maximum dosage of 40 mg once daily ( 2.1 ). Patients greater than 60 years of age, patients with hepatic impairment, and CYP2C19 poor metabolizers: maximum recommended dosage is 20 mg once daily ( 2.2 ). When discontinuing citalopram tablets, reduce dosage gradually ( 2.4 , 5.6 ). 2.1 Recommended Dosage Administer citalopram tablets once daily, with or without food, at an initial dosage of 20 mg once daily, with an increase to a maximum dosage of 40 mg once daily at an interval of no less than one week. Dosages above 40 mg once daily are not recommended due to the risk of QT …
Source: US FDA prescribing information (openFDA / DailyMed), label dated 2025-04-30. Accessed 2026-06-12. US dosing and indications can differ from UK practice — use UK sources for prescribing decisions.
Contraindications
- Hypersensitivity to the active substance or to any of the excipients
- Monoamine oxidase inhibitors (MAOIs) — citalopram should not be given to patients receiving MAOIs, including selegiline in daily doses exceeding 10 mg/day; not to be given for fourteen days after discontinuation of an irreversible MAOI, or for the time specified in the prescribing text of a reversible MAOI (RIMA); MAOIs should not be introduced for seven days after discontinuation of citalopram. Some cases presented with features resembling serotonin syndrome
- Combination with linezolid, unless there are facilities for close observation and monitoring of blood pressure
- Known QT-interval prolongation or congenital long QT syndrome
- Concomitant use with medicinal products known to prolong the QT interval
Side effects
- Somnolence, insomnia and headache (very common); sleep disorder (very common)
- Dry mouth and nausea (very common); diarrhoea, vomiting, constipation, dyspepsia, abdominal pain (common)
- Tremor, paraesthesia, dizziness, disturbance in attention, migraine, amnesia (common)
- Agitation, libido decreased, anxiety, nervousness, confusional state, abnormal orgasm in women, abnormal dreams, apathy (common)
- Palpitations (common); bradycardia and tachycardia (uncommon); QT-prolongation and ventricular arrhythmia including torsade de pointes (not known)
- Increased sweating, tinnitus, yawning and rhinitis (common); hyponatraemia (rare); serotonin syndrome (not known). A dose-response was discovered for increased sweating, dry mouth, insomnia, somnolence, diarrhoea, nausea and fatigue
Interactions
- Monoamine oxidase inhibitors (MAOIs) — increased risk of serotonin syndrome; contraindicated, including MAOIs such as linezolid or intravenous methylene blue
- Pimozide — concomitant use increases plasma concentrations of pimozide, a drug with a narrow therapeutic index, and may increase the risk of QT prolongation and/or ventricular arrhythmias; contraindicated (US label)
- Drugs that prolong the QTc interval — concomitant use can cause additional QT prolongation; avoid concomitant use (US label); contraindicated in the UK SPC §4.3
Clinical monograph
How it works
It selectively inhibits the reuptake of serotonin (5-HT) at the presynaptic neuronal membrane, enhancing central serotonergic activity.
Prescribing in practice
- Citalopram causes dose-dependent QT-interval prolongation; observe the maximum daily dose limits (reduced in older patients and in hepatic impairment) and avoid co-prescribing with other QT-prolonging drugs.
- Risk of hyponatraemia (especially in older patients) and increased gastrointestinal bleeding (consider gastroprotection with concurrent NSAID or anticoagulant).
- Do not stop abruptly, as discontinuation symptoms can occur; taper the dose gradually.
Monitoring
Consider an ECG where there are cardiac risk factors or concurrent QT-prolonging drugs, and correct electrolyte disturbances. Monitor mood and suicidality early in treatment, and check sodium in those at risk of hyponatraemia.
Counselling the patient
- It may take several weeks to feel the full benefit of this medicine.
- Do not stop taking it suddenly; your dose should be reduced gradually.
- Tell your prescriber about all your other medicines, as some can affect your heart rhythm when taken together.
Evidence & guidelines
Guideline-recommended SSRI (NICE NG222); MHRA Drug Safety Update on dose-dependent QT prolongation.
Reference: MHRA Drug Safety Update 2011 (QT Citalopram); NICE CG90 (Depression); Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
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