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Citapad

Citapad (Citalopram 10/20/40 mg) — racemic SSRI for major depression and anxiety. CYP2C19-sensitive — 40 mg cap (20 mg in >60s).

Медицински преглед от Morgan Ellis — Фармацевтичен изследовател · 8 години опит  · Последен преглед: май 2026 г.

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⚡ Quick Answer

Citapad (Citalopram 10 / 20 / 40 mg) is a selective serotonin reuptake inhibitor used for depression, anxiety, and related disorders. Onset of antidepressant effect is gradual — 4–6 weeks for a fair trial.

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How Citapad works

Citapad is a Citalopram-containing SSRI tablet supplied by Cipla. Available strengths: 10 / 20 / 40 mg. Take with or without food, at the same time each day for steady-state plasma levels.

SSRIs block the reuptake of serotonin (5-HT) at the presynaptic serotonin transporter (SERT), increasing synaptic serotonin availability. The therapeutic effect lags transporter blockade by 2–6 weeks — the delay reflects downstream adaptations in 5-HT autoreceptor sensitivity, BDNF expression, and hippocampal neurogenesis, not direct receptor effects. Patients who feel “nothing” at 2 weeks should not stop early; assess response at 4–6 weeks of an adequate dose.

Citalopram is a racemic SSRI — the R-enantiomer adds little antidepressant activity but contributes most of the QT signal. Escitalopram (Lexaheal, the S-enantiomer) achieves the same therapeutic effect at half the dose with substantially less QT risk.

Indications and dosing

IndicationStartingTargetMax
Major depression20 mg OD20–40 mg OD40 mg (20 mg if >60y)
Generalised anxiety / panic10 mg OD × 1 wk20 mg OD40 mg
Older adults / CYP2C19 PM / CYP2C19 inhibitor10 mg OD10–20 mg OD20 mg

Important safety considerations

FDA dose cap — QT prolongation

In 2011 the FDA limited the maximum daily dose of citalopram to 40 mg/day in the general population and 20 mg/day in adults over 60, in CYP2C19 poor metabolisers, and in patients on CYP2C19 inhibitors (omeprazole, esomeprazole, fluvoxamine, cimetidine). Doses above 40 mg cause dose-dependent QT prolongation. If you have congenital long QT, hypokalaemia, hypomagnesaemia, recent MI, or uncompensated heart failure, citalopram is not the right SSRI — sertraline is the closest pharmacological alternative without the QT signal.

Suicidality black-box (under-25)

All SSRIs carry an FDA black-box warning for increased suicidal ideation in patients under 25, particularly in the first 4 weeks and at dose changes. This does не mean SSRIs are net-harmful in young people — meta-analyses show net benefit — but it does mean close clinical monitoring during initiation and titration in adolescents and young adults.

Serotonin syndrome

Combining Citapad with other serotonergic agents can cause serotonin syndrome (tremor, hyperreflexia, clonus, hyperthermia, agitation). Avoid concurrent: MAOIs (14-day washout each direction; fluoxetine needs 5 weeks), tramadol, pethidine, dextromethorphan, linezolid, methylene blue, St John’s wort, MDMA. Triptan + SSRI is generally tolerated for migraine — the absolute risk is low.

Common side effects

  • First 1–2 weeks: nausea, headache, jitteriness/anxiety surge, insomnia or somnolence, loose stools — usually self-limit.
  • Persistent: sexual dysfunction (decreased libido, delayed orgasm/anorgasmia, erectile difficulty — affects up to 50% of men and women on SSRIs; the most common reason for discontinuation), weight changes (modest gain over 6–12 months), bruxism, dry mouth, sweating.
  • Rare but important: hyponatraemia (SIADH, especially in older adults — check Na⁺ at 2 and 4 weeks if at risk), bleeding (additive with NSAIDs/anticoagulants — consider PPI cover), bone-density loss with long-term use.

Drug interactions

Beyond the sub-specific interactions above:

  • NSAIDs / aspirin / anticoagulants — additive bleeding risk; use a PPI for older adults on chronic NSAID + SSRI.
  • Other QT-prolonging drugs (amiodarone, sotalol, methadone, ondansetron, haloperidol, ziprasidone) — additive risk.
  • Lithium — increased serotonin signal; monitor for serotonin syndrome and lithium toxicity.
  • CNS depressants (alcohol, benzodiazepines, opioids) — additive sedation.

Pregnancy, breastfeeding, paediatric

Most SSRIs are category C in pregnancy with an acceptable risk-benefit profile when depression itself poses real harm. Paroxetine is the exception — first-trimester exposure linked to small absolute increases in cardiac malformations. Sertraline is generally regarded as the SSRI of choice in pregnancy and lactation. Late-third-trimester SSRI exposure can produce a transient neonatal adaptation syndrome (jitteriness, feeding difficulty) that typically resolves within 1–2 weeks. Discuss any change in pregnancy with the prescriber — abruptly stopping during pregnancy carries its own risk (relapse).

Storage

Store at 15–30 °C in a dry place, away from direct sunlight and out of reach of children.

Често задавани въпроси

How long until Citapad works?

Some patients notice early effects on sleep and anxiety within 1–2 weeks, but the full antidepressant or anti-anxiety effect typically takes 4–6 weeks at an adequate dose. Don’t conclude Citapad isn’t working until you’ve had at least 4 weeks at a therapeutic dose.

Can I drink alcohol on Citapad?

Alcohol does not chemically interact with SSRIs in a dangerous way at moderate consumption, but it worsens the underlying depression and amplifies SSRI sedation. Many psychiatrists advise minimising alcohol during the first 4–8 weeks while the effect is being established.

Will Citapad change my personality?

No. Adequately-treated patients describe feeling more like themselves, not less. If you feel emotionally blunted, sexually disconnected, or detached after several weeks, raise this with your prescriber — it can be dose-related or medication-specific and is often manageable.

What if I miss a dose?

Take it as soon as you remember the same day. If it’s nearly time for the next dose, skip the missed one. Never double up. With short-half-life SSRIs (paroxetine, fluvoxamine), a missed dose can produce mild withdrawal — take it as soon as you remember.

Can I stop Citapad when I feel better?

No — stopping after 4–6 weeks of feeling better is the most common cause of relapse. Most guidelines recommend continuing an effective antidepressant for at least 6–12 months after full remission of the first episode, longer for recurrent depression or anxiety. Always taper rather than stopping abruptly.

Does Citapad cause weight gain?

Most SSRIs cause modest weight gain over 6–12 months (often 2–4 kg). Fluoxetine is the most weight-neutral or even mildly weight-reducing of the SSRIs in some studies. If weight gain is a major concern, this is worth discussing with the prescriber when choosing or switching.

Can Citapad be combined with therapy?

Combination of an SSRI plus structured psychotherapy (CBT for depression and anxiety; ERP for OCD) consistently outperforms either alone in moderate-to-severe disease. Medication addresses biological dysregulation; therapy addresses cognitive and behavioural patterns.

How do I taper Citapad?

For most SSRIs, taper over 4–8 weeks by halving the dose every 2 weeks. Paroxetine and fluvoxamine require slower tapers (often 8–12 weeks) because of their short half-lives. Some patients need hyperbolic tapering (10% reductions every 2–4 weeks) at the bottom end. The prescriber should plan this with you.

Is Citapad addictive?

SSRIs are not addictive in the substance-use-disorder sense — there’s no euphoric effect, no compulsive use, and no escalating tolerance. They do produce physical dependence: abrupt cessation causes withdrawal (discontinuation syndrome). That dependence is not addiction; it is a predictable pharmacological adaptation that resolves with proper taper.

What if I want to switch antidepressants?

Most SSRI-to-SSRI switches use a direct cross-taper or short washout. Switching to or from an MAOI requires a strict washout (14 days; 5 weeks if coming off fluoxetine because of its long half-life) to avoid serotonin syndrome. Switching is a clinician-supervised decision.

Other Mental Health Medications

Medical disclaimer. This page is educational and is not a substitute for individualised medical advice. Mental-health pharmacotherapy should be initiated, monitored, and adjusted under a qualified clinician. If you or someone you know is in suicidal crisis, contact local emergency services immediately, or call your country’s suicide-prevention helpline (US/Canada: 988; UK: Samaritans 116 123; international list: findahelpline.com).

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