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 mild or moderate renal impairment. No information is available in severe renal impairment (creatinine clearance below 20 ml/min) (section 4.2). Caution should be used in patients with reduced kidney function (section 4.4).
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 citalopram or to any of the excipients
- Monoamine oxidase inhibitors (MAOIs), including selegiline in daily doses exceeding 10 mg/day - do not give citalopram to patients receiving MAOIs; allow 14 days after stopping an irreversible MAOI (or the interval specified for a reversible MAOI) before starting citalopram, and 7 days after stopping citalopram before introducing an MAOI
- 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 that are known to prolong the QT interval
Side effects
- Sleep disorder, somnolence and insomnia (very common)
- Headache (very common)
- Nausea and dry mouth (very common)
- Agitation, anxiety, nervousness, decreased libido and abnormal dreams (common)
- Tremor, paraesthesia, dizziness and disturbance in attention (common)
- Increased sweating, decreased appetite, palpitations, and sexual dysfunction including impotence and ejaculation disorder (common)
- QT prolongation and ventricular arrhythmia including torsade de pointes, and hyponatraemia (frequency rare / not known)
Interactions
- MAOIs including selegiline - contraindicated, risk of serotonin syndrome (section 4.3)
- Linezolid - contraindicated unless facilities exist for close observation and blood pressure monitoring (section 4.3)
- Medicinal products known to prolong the QT interval - contraindicated (section 4.3)
- US label cross-check: pimozide is contraindicated (increased pimozide plasma concentrations and risk of QT prolongation / ventricular arrhythmias)
- US label cross-check: CYP2C19 inhibitors - maximum recommended dosage 20 mg once daily
- US label cross-check: aspirin, NSAIDs, other antiplatelet drugs, warfarin and other anticoagulants - increased risk of bleeding
- NOTE: the SPC section 4.5 interactions section itself was not captured in this bundle; the UK entries above are drawn from section 4.3
Clinical monograph
How it works
It selectively inhibits serotonin reuptake, increasing synaptic serotonin over several weeks.
Prescribing in practice
- It causes dose-related QT-interval prolongation, so maximum doses are capped — lower in older patients and in hepatic impairment (MHRA); avoid with other QT-prolonging drugs.
- Watch for hyponatraemia and an increased bleeding risk in older patients, especially with NSAIDs or antithrombotics.
- Risk of serotonin syndrome with other serotonergic drugs.
Monitoring
Review mood and suicidal ideation early; check sodium if features of hyponatraemia develop; consider ECG where QT risk is high.
Counselling the patient
- It can take a few weeks to work, and anxiety may briefly increase at first.
- Do not stop suddenly.
- Report palpitations, and worsening mood or thoughts of self-harm.
Evidence & guidelines
A first-line SSRI for depression (NICE NG222), with MHRA maximum-dose limits because of QT prolongation.
Reference: MHRA Drug Safety Update 2011 (citalopram QT); NICE CG90 (Depression); AGS Beers Criteria 2023; 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).
Related
Curated clinical cross-links plus same-class fallbacks.
- Falls Assessment in Older Adults · NICE CG161 2013
- Delirium Outside ICU · NICE CG103
- Comprehensive Geriatric Assessment (CGA) · BGS / NICE
- Delirium Assessment and Management · NICE CG103 2010
- Frailty Recognition and Management · BGS Frailty Framework / NHS NHSE
- Polypharmacy and Medicines Optimisation · STOPP/START v2 2014 / NICE NG5