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Paxil alcohol interaction. Eater and incidence for PAXIL CR at least twice that for placebo, derived from Table 5) were: Nausea, asthenia, libido decreased, somnolence, insomnia, female genital disorders, sweating, dizziness, diarrhea, and constipation. In the luteal phase dosing PMDD trial, which employed dosing of 12.5 mg day or 25 mg day of PAXIL CR limited to the 2 weeks prior to the onset of menses over 3 consecutive menstrual cycles, adverse events were evaluated during the first 14 days of each off-drug phase. When the 3 off-drug phases were combined, the following adverse events were reported at an incidence of 2% or greater for PAXIL CR and were at least twice the rate of that reported for placebo: Infection (5.3% versus 2.5%), depression (2.8% versus 0.8%), insomnia (2.4% versus 0.8%), sinusitis (2.4% versus 0%), and asthenia (2.0% versus 0.8%). Incidence in Controlled Clinical Trials: Table 1 enumerates adverse events that occurred at an incidence of 1% or more among patients treated with PAXIL CR, ag paxil alcohol

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Ed 18 to 65, who participated in 2 short-term (12-week) placebo-controlled trials in major depressive disorder in which patients were dosed in a range of 25 mg to 62.5 mg day. Table 2 enumerates adverse events reported at an incidence of 5% or greater among elderly patients (ages 60 to 88) treated with PAXIL CR who participated in a short-term (12-week) placebo-controlled trial in major depressive disorder in which patients were dosed in a range of 12.5 mg to 50 mg day. Table 3 enumerates adverse events reported at an incidence of 1% or greater among patients (19 to 72 years) treated with PAXIL CR who participated in short-term (10-week) placebo-controlled trials in panic disorder in which patients were dosed in a range of 12.5 mg to 75 mg day. Table 4 enumerates adverse events reported at an incidence of 1% or greater among adult patients treated with PAXIL CR who participated in a short-term (12-week), double-blind, placebo-controlled trial in social anxiety disorder in which patient paxil alcohol

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paxil alcohol interaction & 179; 1% of Patients Treated With PAXIL CR in a Pool of 2 Studies in Major Depressive Disorder1 paxil alcohol interaction, 2 Body System Adverse Event % Reporting Event PAXIL CR (n = 212) Placebo (n = 211) Body as a Whole Headache 27% 20% Asthenia 14% 9% Infection3 8% 5% Abdominal Pain 7% 4% Back Pain 5% 3% Trauma4 5% 1% Pain5 3% 1% Allergic Reaction6 2% 1% Cardiovascular System Tachycardia 1% 0% Vasodilatation7 2% 0% Digestive System Nausea 22% 10% Diarrhea 18% 7% Dry Mouth 15% 8% Constipation 10% 4% Flatulence 6% 4% Decreased Appetite 4% 2% Vomiting 2% 1% Nervous System Somnolence 22% 8% Insomnia 17% 9% Dizziness 14% 4% Libido Decreased 7% 3% Tremor 7% 1% Hypertonia 3% 1% Paresthes paxil alcohol interaction.

paxil alcohol interaction Ia 3% 1% Agitation 2% 1% Confusion 1% 0% Respiratory System Yawn 5% 0% Rhinitis 4% 1% Cough Increased 2% 1% Bronchitis 1% 0% Skin and Appendages Sweating 6% 2% Photosensitivity 2% 0% Special Senses Abnormal Vision8 5% 1% Taste Perversion 2% 0% Urogenital System Abnormal Ejaculation9 paxil alcohol interaction, 10 26% 1% Female Genital Disorder9 paxil alcohol interaction, 11 10% <1% Impotence9 5% 3% Urinary Tract Infection 3% 1% Menstrual Disorder9 2% <1% Vaginitis9 2% 0% 1.Adverse events for which the PAXIL CR reporting incidence was less than or equal to the placebo incidence are not included. These events are: Abnormal dreams paxil alcohol interaction, anxiety paxil alcohol interaction, arthralgia paxil alcohol interaction, depersonalization paxil alcohol interaction, dysmenorrhea paxil alcohol interaction, dyspepsia paxil alcohol interaction, hyperkinesia paxil alcohol interaction, increased appetite paxil alcohol interaction, myalgia paxil alcohol interaction, nervousness paxil alcohol interaction, pharyngitis paxil alcohol interaction, purpura paxil alcohol interaction, rash paxil alcohol interaction, respiratory disorder paxil alcohol interaction, sinusitis paxil alcohol interaction, urinary frequency paxil alcohol interaction, and weight gain. 2.<1% means greater than zero and less than 1%. 3.Mostly flu. 4.A wide variety of injuries with no obvious pattern. 5.Pain in a variety of locations with no obvious pattern. 6.Most frequently seasonal allergic symptoms. 7.Usually flushing. 8.Mostly blurred vision. 9. Based on the number of males or females. 10. Mostly anorgasmia or delayed ejaculation. 11. Mostly anorgasmia or delayed orgasm. Table 2. Treatment-Emergent Adverse Events Occurring in & 179; 5% of Patients Treated With PAXIL CR in a Study of Elderly Patien.

paxil alcohol interaction Increased appetite paxil alcohol interaction, myalgia paxil alcohol interaction, nervousness paxil alcohol interaction, pharyngitis paxil alcohol interaction, purpura paxil alcohol interaction, rash paxil alcohol interaction, respiratory disorder paxil alcohol interaction, sinusitis paxil alcohol interaction, urinary frequency paxil alcohol interaction, and weight gain. 2.<1% means greater than zero and less than 1%. 3.Mostly flu. 4.A wide variety of injuries with no obvious pattern. 5.Pain in a variety of locations with no obvious pattern. 6.Most frequently seasonal allergic symptoms. 7.Usually flushing. 8.Mostly blurred vision. 9. Based on the number of males or females. 10. Mostly anorgasmia or delayed ejaculation. 11. Mostly anorgasmia or delayed orgasm. Table 2. Treatment-Emergent Adverse Events Occurring in & 179; 5% of Patients Treated With PAXIL CR in a Study of Elderly Patient.

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Uch an interaction with PAXIL, limited animal data on the effects of combined use of paroxetine and MAOIs suggest that these drugs may act synergistically to elevate blood pressure and evoke behavioral excitation. Therefore, it is recommended that PAXIL not be used in combination with an MAOI, or within 14 days of discontinuing treatment with an MAOI. At least 2 weeks should be allowed after stopping PAXIL before starting an MAOI. Potential Interaction With Thioridazine:Thioridazine administration alone produces prolongation of the QTc interval, which is associated with serious ventricular arrhythmias, such as torsade de pointes– type arrhythmias, and sudden death. This effect appears to be dose related. An in vivo study suggests that drugs which inhibit P450IID6, such as paroxetine, will elevate plasma levels of thioridazine. Therefore, it is recommended that paroxetine not be used in combination with thioridazine (see CONTRAINDICATIONS and PRECAUTIONS). Page: 1 2 3 4 5 6 7 Next >>Related WebsitesBipolarConnect.com - Information on bipolar disorder: signs and symptoms, mental health, risks, treatments and other information on bipolar disorder.MyDepressionConnection.com - Learn about the types of depression and their signs, depression in teens, children, and elderly, treating depression, and depression drugs. Get depression help from blogs and depression support forums. Visit Our Health Centers * All Health Centers * Acne Addictions AIDS HIV Alcohol Abuse Allergies Alternative Medicine Alzheimer's Arthritis Asthma Attention Deficit Disorder (ADHD) Backache Bipolar A

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