Skip to content
ClinCalc Pro
Menu
SSRI (Selective Serotonin Reuptake Inhibitor) Pregnancy: §4.6: Published data on pregnant women (more than 2500 exposed outcomes) indicate no malformative foeto/neonatal toxicity; however, citalopram SHOULD NOT BE USED during pregnancy unless clearly necessary and only after careful consideration of risk/benefit. Abrupt discontinuation should be avoided during pregnancy. Neonates should be observed if maternal use continues into the later stages of pregnancy, particularly the third trimester — symptoms may include respiratory distress, cyanosis, apnoea, seizures, temperature instability, feeding difficulty, vomiting, hypoglycaemia, hypertonia, hypotonia, hyperreflexia, tremor, jitteriness, irritability, lethargy, constant crying, somnolence and difficulty sleeping, in the majority of cases beginning within 24 hours after delivery. SSRI use in late pregnancy may increase the risk of persistent pulmonary hypertension of the newborn (approximately 5 cases per 1000 pregnancies, against 1-2 per 1000 in the general population). Observational data indicate an increased risk (less than 2-fold) of postpartum haemorrhage.

Citalopram

Brand names: Cipramil

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: 20 mg daily as a single oral dose (major depressive episodes)
Route: Oral
Frequency: Once daily as a single daily dose; can be taken at any time of the day without regard to food intake
Max: 40 mg daily. In elderly patients (>65 years) the recommended maximum is 20 mg daily. In mild or moderate hepatic impairment and in CYP2C19 poor metabolisers the maximum is 20 mg daily
Source: UK SPC (eMC) for Cipramil 20 mg film-coated tablets, §4.2 (https://www.medicines.org.uk/emc/product/992/smpc). MAJOR DEPRESSIVE EPISODES: 20 mg daily as a single oral dose; dependent on individual patient response the dose may be increased to a maximum of 40 mg daily. In general improvement starts after one week but may only become evident from the second week of therapy; dosage should be reviewed and adjusted if necessary within 3 to 4 weeks of initiation and thereafter as judged clinically appropriate. Although there may be an increased potential for undesirable effects at higher doses, if after some weeks on the recommended dose insufficient response is seen, some patients may benefit from an increase up to a maximum of 40 mg a day. Dosage adjustments should be made carefully on an individual patient basis, to maintain the patient at the lowest effective dose. Patients with depression should be treated for a sufficient period of at least 6 months to ensure they are free from symptoms. PANIC DISORDER: a single oral dose of 10 mg is recommended for the first week before increasing to 20 mg daily; dependent on response the dose may be increased to a maximum of 40 mg daily, gradually in 10 mg steps. A low initial starting dose is recommended to minimise the potential worsening of panic symptoms, which is generally recognised to occur early in treatment of this disorder. Patients with panic disorder should be treated for a sufficient period to ensure they are free from symptoms — this period may be several months or even longer. ELDERLY (>65 years): the dose should be decreased to half of the recommended dose, e.g. 10-20 mg daily, with a recommended maximum of 20 mg daily. HEPATIC IMPAIRMENT: an initial dose of 10 mg daily for the first two weeks is recommended in mild or moderate impairment, which may be increased to a maximum of 20 mg daily depending on response; caution and extra careful dose titration in severely reduced hepatic function. CYP2C19 POOR METABOLISERS: an initial dose of 10 mg daily during the first two weeks is recommended, which may be increased to a maximum of 20 mg daily depending on response. PAEDIATRIC: citalopram should NOT be used in the treatment of children and adolescents under the age of 18 years — hence paedDose is null. Verify any under-18 use against a children's formulary. WITHDRAWAL: abrupt discontinuation should be avoided; the dose should be gradually reduced over a period of at least one to two weeks to reduce the risk of withdrawal reactions; if intolerable symptoms occur, resuming the previously prescribed dose may be considered, then decreasing at a more gradual rate. Note: §4.5 was not retrieved in this bundle — the interactions listed below are taken from §4.3 of the UK SPC and from the US label; verify the full §4.5.

Dose adjustments

Renal

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 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 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).

Related

Curated clinical cross-links plus same-class fallbacks.