מדינה: הממלכה המאוחדת
שפה: אנגלית
מקור: MHRA (Medicines & Healthcare Products Regulatory Agency)
Citalopram hydrobromide
A A H Pharmaceuticals Ltd
N06AB04
Citalopram hydrobromide
10mg
Oral tablet
Oral
No Controlled Drug Status
Valid as a prescribable product
BNF: 04030300; GTIN: 5037563005031
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS MEDICINE BECAUSE IT CONTAINS IMPORTANT INFORMATION FOR YOU. - Keep this leaflet. You may need to read it again. - If you have any further questions, ask your doctor, pharmacist or nurse. - This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. - If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4. WHAT IS IN THIS LEAFLET 1. What Citalopram Tablets are and what are they used for 2. What you need to know before you take Citalopram Tablets 3. How to take Citalopram Tablets 4. Possible side effects 5. How to store Citalopram Tablets 6. Contents of the pack and other information 1. WHAT CITALOPRAM TABLETS ARE AND WHAT ARE THEY USED FOR How does Citalopram work? Citalopram is a Selective Serotonin Reuptake Inhibitor (SSRI) and belongs to a group of medicines known as antidepressants. These medicines help to correct certain chemical imbalances in the brain that are causing the symptoms of your illness. What is Citalopram used for? Citalopram contains citalopram and is used for the treatment of depression and, when you feel better, to help prevent these symptoms recurring. Citalopram is also used for long-term treatment to prevent the occurrence of new episodes of depression if you have recurrent depression. Citalopram is also beneficial in relieving symptoms if you tend to suffer from panic attacks with or without agoraphobia (e.g. fear of leaving the house, entering shops, or fear of public places). 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE CITALOPRAM TABLETS DO NOT TAKE CITALOPRAM TABLETS: - If you are allergic to citalopram or any of the other ingredients of this medicine (listed in section 6). An allergic reaction may include rash, itching, swelling of face, lips or hands/feet, or breathing difficulties. - If you are taking medicines called monoamine oxidase inhi קרא את המסמך השלם
1. NAME OF THE MEDICINAL PRODUCT Citalopram 10 mg Tablets. 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each tablet contains 10 mg citalopram, as citalopram hydrobromide. Excipient(s) with known effect: Each 10 mg tablet contains 13.3 mg of lactose monohydrate For the full list of excipients, see 6.1. 3. PHARMACEUTICAL FORM Film-coated Tablet. White, round, flat, bevelled, film-coated tablet. 4. CLINICAL PARTICULARS 4.1. THERAPEUTIC INDICATIONS Treatment of depressive illness in the initial phase and as maintenance against potential relapse/recurrence. Citalopram is also indicated in the treatment of panic disorder with or without agoraphobia. 4.2 POSOLOGY AND METHOD OF ADMINISTRATION TREATING DEPRESSION: _Adults: _ Citalopram should be administered as a single oral dose of 20 mg daily. Dependent on individual patient response, the dose may be increased to a maximum of 40 mg daily. In general, improvement in patients starts after one week, but may only become evident from the second week of therapy. As with all antidepressant medicinal products, dosage should be reviewed and adjusted, if necessary, within 3 to 4 weeks of initiation of therapy 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 having their dose increased up to a maximum of 40 mg a day (see section 5.1). Dosage adjustments should be made carefully on an individual patient basis, to maintain the patient at the lowest effective dose. A treatment period of at least 6 months is usually necessary to provide adequate maintenance against the potential for relapse. TREATING PANIC DISORDER: _Adults: _ In common with other pharmacotherapy used in this patient group, a low starting dose is advised to reduce the likelihood of a paradoxical initial anxiogenic effect. A single oral dose of 10 mg is recommended for the first week before increasing the dose to 20 mg daily. Depend קרא את המסמך השלם