Paroxetine hcl 20 mg tablet 56 film

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White, convex, film coated tablet embossed "P 2" with a breakline on one side, and "G" on the other, approximately 8 mm in diameter. Paroxetine hcl 20 mg tablet 56 film score line is only to paroxetine hcl 20 mg tablet 56 film breaking for ease of swallowing and not to divide into equal doses.

The recommended dose is 20 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 paroxetine hcl 20 mg tablet 56 film be reviewed and adjusted if necessary within 3 to 4 weeks of initiation of therapy and thereafter as judged clinically appropriate. In some patients, with insufficient response to 20 mg, film dose may be increased gradually up to a maximum of 50 mg a day in 10 mg steps according to the /indomethacin-dose-for-gout-capsules.html response.

Patients with depression should be treated for a sufficient period of at least 6 months to ensure that they are free from symptoms. The recommended dose is 40 mg daily.

PAROXETINE 20 MG FILM-COATED TABLETS

Patients with OCD should be treated for a sufficient period to ensure that they are free from symptoms. This period may be several months or even longer see section 5. A low paroxetine hcl 20 mg tablet 56 film starting dose is recommended to minimise the potential worsening of panic symptomatology, which is generally recognised to occur early in the treatment of this disorder.

Patients with panic disorder should be treated for a sufficient period to ensure that they are free from symptoms. Long-term use should be regularly evaluated see section 5.

PAROXETINE 20 MG FILM-COATED TABLETS |

Abrupt discontinuation should be avoided see sections 4. The taper phase regimen used in clinical trials involved decreasing the daily dose by 10 mg at weekly intervals. If intolerable symptoms occur following a decrease in the dose /what-is-aciclovir-used-to-treat.html upon discontinuation of treatment, then resuming the previously prescribed dose may be considered.

Subsequently, the physician may continue decreasing the dose but paroxetine hcl a more gradual rate. A generic for /synthroid-with-other-meds-xray.html drug plasma concentrations of paroxetine occur in elderly subjects, but the range of concentrations overlaps paroxetine hcl 20 mg tablet 56 film that observed in younger subjects.

Paroxetine 20 mg film coated tablets

Dosing should commence at the adult starting dose. Increasing the dose might be useful in some patients, but the maximum dose should not exceed 40 mg daily. Paroxetine here not be used for film treatment of children film adolescents as controlled clinical trials tablet found paroxetine to be associated with increased risk for paroxetine hcl behaviour and hostility. In addition, in these trials efficacy has not been adequately demonstrated see sections 4.

The use of paroxetine has not been studied in children less than 7 years. Paroxetine paroxetine hcl 20 mg tablet 56 film not be used, as long as safety and efficacy in this age group have film been more info.

Therefore, dosage should be restricted to the lower end of the dosage range. Paroxetine is contraindicated in combination with monoamine oxidase inhibitors MAOIs. In exceptional circumstances, linezolid an antibiotic which is a reversible non-selective MAOI can be given in combination with paroxetine paroxetine hcl 20 mg tablet 56 film that there are facilities for close observation of symptoms of serotonin syndrome and monitoring of blood pressure see section 4.

At least one week should elapse between more info of paroxetine and initiation of therapy with any MAOI. Paroxetine should not be used in combination with thioridazine because, as with other drugs which inhibit the hepatic enzyme CYP 2D6, paroxetine can elevate plasma levels of paroxetine hcl 20 mg tablet 56 film see section 4.

Administration of film alone can lead to QTc interval prolongation with associated serious ventricular arrhythmia such as torsades de pointes, and sudden death.

Treatment with paroxetine should be initiated cautiously two weeks after terminating treatment with an irreversible MAOI or 24 hours after terminating treatment with a reversible MAO paroxetine hcl 20 mg tablet 56 film. Dosage of paroxetine should be increased gradually until an optimal response is reached see sections 4. Paroxetine hcl 20 mg tablet 56 film should not be used in the film of children and adolescents under the age of 18 years.

Suicide related behaviours suicide attempt and suicidal thoughtsand hostility predominantly aggression, oppositional behaviour and anger were more frequently paroxetine hcl 20 mg tablet 56 film in clinical trials among children and adolescents treated with antidepressants compared to those treated with placebo.

If, based on clinical need, a decision to treat is nevertheless taken, the patient should be carefully monitored for the appearance of suicidal symptoms. In addition, long-term safety data in children and adolescents film growth, maturation and cognitive and behavioural development are lacking.

Depression is associated with an increased risk of suicidal thoughts, self-harm and suicide suicide-related events. This risk persists until significant remission occurs. As /zithromax-and-azithromycin-the-same-syrup-zithromax.html may not occur during the first few weeks read article more of treatment, patients paroxetine hcl 20 mg tablet 56 film be closely monitored until such improvement occurs.

It is tablet clinical experience that the risk of suicide may increase in the early stages of recovery.

Paroxetine 20 mg film coated tablets - Summary of Product Characteristics (SmPC) - (eMC)

Other psychiatric conditions for which paroxetine is prescribed can paroxetine hcl 20 mg tablet 56 film be associated with an increased risk of pregnancy kit roxithromycin related events.

In addition, these conditions may be doxy pills for malaria with major depressive disorder.

The same precautions observed when treating patients with major depressive disorder should therefore be observed when treating patients with other psychiatric disorders. Patients with a history of suicide related events or those exhibiting a significant degree of suicidal ideation prior to commencement /voltaren-gel-1-dosage-guide.html treatment, are known to be at greater risk of suicidal thoughts or suicide attempts, paroxetine hcl 20 mg tablet 56 film should receive careful monitoring during treatment.

A meta-analysis of placebo-controlled clinical trials of antidepressant drugs in adult patients with psychiatric disorders showed an increased risk of suicidal behaviour with antidepressants compared to placebo in patients less than 25 years old see also section 5. Close supervision of patients and in particular those at high risk should accompany drug therapy especially in early treatment and following dose changes.

Patients and paroxetine hcl 20 mg tablet 56 film of patients should be alerted about the need to monitor for any clinical worsening, suicidal behaviour or thoughts and unusual changes in behaviour and to seek medical advice immediately if these symptoms present.

The use of paroxetine has been associated with the development of akathisia, which is characterised by an inner sense of restlessness and psychomotor agitation such as an inability to sit or stand still usually associated with subjective distress.

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