Product image of Goldamit (Citalopram) supplied by GNH India

Goldamit

Active Ingredient:
Citalopram
Origin:
EU

Goldamit (Citalopram)

Goldamit is a prescription oral medication that contains the active ingredient citalopram, a selective serotonin reuptake inhibitor (SSRI) used as an antidepressant. It is marketed in the European Union and is supplied in tablet form, though specific strength information is not disclosed here. As an SSRI, Goldamit works by increasing serotonin levels in the brain to help improve mood and emotional balance and overall well‑being.

Manufacturer / TM Owner

Panagiotis Leon & Co

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Indications & Clinical Uses

Goldamit (citalopram) is primarily prescribed for the treatment of major depressive disorder and may be considered in related mood conditions.

  • Management of major depressive disorder in adults.
  • Adjunctive therapy for persistent depressive symptoms when first‑line treatment is insufficient.
  • Off‑label use for anxiety disorders under clinical supervision.
  • May be used in the continuation phase to prevent relapse after acute response.
  • Treatment of depressive episodes in bipolar disorder under specialist supervision.
  • May be considered for obsessive‑compulsive disorder when other options are ineffective.

Side Effects

Side effects of Goldamit vary in frequency and severity; they are categorized as common or serious, and patients should be aware of both typical and rare reactions.

Common

  • Nausea or upset stomach.
  • Dry mouth.
  • Drowsiness or fatigue.
  • Insomnia or vivid dreams.
  • Sweating.
  • Sexual dysfunction such as decreased libido.
  • Headache.
  • Dizziness.

Serious

  • Serotonin syndrome (agitation, rapid heart rate, high blood pressure).
  • Severe allergic reaction (rash, swelling, difficulty breathing).
  • QT interval prolongation leading to cardiac arrhythmia.
  • Suicidal thoughts, especially in young adults.
  • Severe hyponatremia (low sodium levels).
  • Cardiac arrhythmias requiring medical attention.

Precautions & Warnings

Before starting Goldamit, healthcare providers assess several safety considerations to minimize risks and ensure appropriate monitoring throughout treatment.

  • Evaluate history of bipolar disorder or mania.
  • Review any previous serotonin syndrome episodes.
  • Assess liver or kidney impairment that may affect drug clearance.
  • Consider pregnancy, breastfeeding, and potential fetal risk.
  • Monitor for worsening depression or emergence of suicidal thoughts.
  • Use caution in patients taking other QT‑prolonging agents.
  • Review concomitant use of over‑the‑counter supplements that may affect serotonin levels (e.g., St. John’s wort).

Avoid Interactions

Goldamit can interact with other medicines; some combinations should be avoided while others require careful monitoring to prevent adverse effects.

Avoid

  • Monoamine oxidase inhibitors (MAOIs) or within 14 days of stopping an MAOI.
  • Other serotonergic agents such as tramadol, linezolid, or certain migraine medications.
  • Drugs known to prolong the QT interval (e.g., certain antiarrhythmics).
  • Certain antifungal agents (e.g., ketoconazole) that increase citalopram levels.

Use with caution

  • Anticoagulants like warfarin (may increase bleeding risk).
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) that can affect platelet function.
  • Alcohol, which may enhance drowsiness.
  • Anticonvulsants such as carbamazepine that may reduce citalopram efficacy.
  • Other QT‑prolonging medications under close cardiac monitoring.

Frequently Asked Questions

Goldamit is primarily prescribed for the treatment of major depressive disorder in adults.

Goldamit inhibits the reuptake of serotonin into presynaptic neurons, increasing extracellular serotonin levels that help regulate mood.

Common side effects include nausea, dry mouth, drowsiness, insomnia, sweating, sexual dysfunction, headache, and dizziness.

In rare cases, Goldamit may prolong the QT interval, which can lead to cardiac arrhythmias; monitoring is advised for at‑risk patients.

Combining Goldamit with other serotonergic antidepressants can increase the risk of serotonin syndrome and should generally be avoided.

Inform your doctor about any history of bipolar disorder, heart problems, liver or kidney disease, pregnancy, breastfeeding, and all current medications or supplements.

Therapeutic effects may begin to appear within 2 to 4 weeks, but full benefit often requires 6 to 8 weeks of consistent use.

There are no specific dietary restrictions, but excessive alcohol consumption can increase drowsiness and should be limited.

Watch for agitation, rapid heart rate, high blood pressure, fever, muscle rigidity, or confusion and seek medical attention immediately if they occur.

The safety of Goldamit during pregnancy or breastfeeding has not been definitively established; discuss potential risks and benefits with your healthcare provider.

Alcohol may enhance drowsiness and impair judgment when taken with Goldamit, so moderate or avoid alcohol consumption.

Regular follow‑up appointments to assess mood, side effects, suicidal thoughts, and periodic ECG monitoring for patients at risk of QT prolongation are recommended.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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