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SSRI Antidepressant Pregnancy: Published data on more than 2500 exposed pregnancies indicate no malformative foeto/neonatal toxicity, however citalopram should not be used during pregnancy unless clearly necessary and only after careful risk/benefit consideration. Observe neonates if maternal use continues into later pregnancy, particularly the third trimester (respiratory distress, cyanosis, apnoea, seizures, feeding difficulty, hypoglycaemia, tremor, irritability and other symptoms have been reported). Avoid abrupt discontinuation during pregnancy. Increased risk (less than 2-fold) of postpartum haemorrhage with SSRI/SNRI exposure in the month before birth, and a possible increased risk of persistent pulmonary hypertension of the newborn. Citalopram is excreted in breast milk (about 5% of the weight-related maternal daily dose); discontinuation of breast-feeding should be considered and caution is recommended.

Citalopram

Brand names: Cipramil

Used in: Depression & Anxiety

Citalopram is a selective serotonin reuptake inhibitor (SSRI) used for depression and panic disorder.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: Elderly patients (over 65 years of age): the dose should be decreased to half of the recommended dose, e.g. 10-20 mg daily. (Standard adult dose for depression: a single oral dose of 20 mg daily, which may be increased depending on individual response to a maximum of 40 mg daily.)
Route: Oral - a single daily dose, which can be taken at any time of day without regard to food
Frequency: Once daily
Max: 20 mg daily in the elderly (over 65 years). In younger adults the maximum is 40 mg daily.
PANIC DISORDER (adults): a single oral dose of 10 mg is recommended for the first week before increasing to 20 mg daily; the dose may be increased in 10 mg steps according to response to a maximum of 40 mg daily, although an optimum dose of 20-30 mg daily was indicated in a clinical study. A low starting dose reduces the likelihood of a paradoxical initial anxiogenic effect. DEPRESSION: improvement generally starts after one week but may only become evident from the second week; dosage should be reviewed and adjusted within 3 to 4 weeks of initiation and thereafter as clinically appropriate; patients should be treated for at least 6 months to ensure they are free from symptoms. Maintain the patient at the lowest effective dose. HEPATIC IMPAIRMENT: an initial dose of 10 mg daily for the first two weeks is recommended in mild or moderate hepatic impairment, increasing if needed to a maximum of 20 mg daily; caution and extra careful titration in severely reduced hepatic function. CYP2C19 POOR METABOLISERS: initial dose 10 mg daily for the first two weeks, increasing if needed to a maximum of 20 mg daily. DISCONTINUATION: avoid abrupt discontinuation - reduce the dose gradually over at least one to two weeks; if intolerable symptoms occur, consider resuming the previous dose and then decreasing more gradually. CHILDREN AND ADOLESCENTS UNDER 18 YEARS: citalopram should not be used - no paediatric dose is stated. CAUTION is advised in the treatment of elderly patients and patients with reduced kidney and liver function (section 4.4). US label cross-check (may differ from UK): maximum recommended dosage is 20 mg once daily for patients over 60 years of age, patients with hepatic impairment, CYP2C19 poor metabolisers, and when used concomitantly with a CYP2C19 inhibitor.

Dose adjustments

Renal

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 UK

Administer 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.