Buy Paxil online from Canada Drugs, an online Canadian Pharmacy that offers free shipping on all orders of discount Paxil. Paroxetine is used treat depression, obsessive-compulsive disorder and anxiety disorders. Learn about side effects, interactions and indications. Paxil is the brand name for the antidepressant paroxetine. Though doctors prescribe Paxil to treat depression, it s also used to treat anxiety disorders including. A generic drug is a copy of the brand-name drug with the same dosage, safety, strength, quality, how it is taken, performance, and intended use. Before generics become available on the market, the generic company must prove it has the same active ingredients as the brand-name and works the same way in the body in the same amount of time. The only differences between generics and their brand-name counterparts is the generics are less expensive and may look slightly different (e.g. different shape or color), as trademark laws prevent a generic from looking exactly like the brand-name drug. Generics are less expensive because generic manufacturers don't have to invest large sums of money to invent a drug. When the brand-name patent expires, generic companies can manufacture a copy of the brand-name drug and sell it at substantial discounts. (Rx) - indicates only available by prescription Paxil Description Paxil is an antidepressant classed as a 'serotonin selective reuptake inhibitor' (SSRI). Paxil contains the active ingredient called paroxetine, which works to block the clearance of serotonin in brain cells. Depression is associated with an imbalance of serotonin, and thus SSRIs may alleviate the symptoms of depression by regulating serotonin levels in the brain. SSRIs have also been shown to help manage other conditions, such as obsessive compulsive disorder (OCD), panic attacks, and generalized anxiety disorders. Paroxetine may also be prescribed for other medical conditions, such as severe premenstrual syndrome (premenstrual dysphoric disorder), premature ejaculation, diabetic neuropathies, chronic headaches, or post-traumatic stress disorder (PTSD). Paxil Directions Please take this medicine as directed by your doctor. If it comes with an information leaflet, please read this carefully and clarify and queries with your doctor, nurse or pharmacist. Please store paroxetine at room temperature at 77 degrees F (25 degrees C) in a tightly closed container, and also away from direct heat or light. If required, this medicine may be temporarily stored between 59-86 degrees F (15-30 degrees C). Take this medication regularly, do not miss any doses, and do not stop taking this medicine even if you feel better. If you miss a morning dose, then take your dose in the afternoon if you remember. If you don't remember until the next morning, then skip your missed dose and carry on with your regular dose schedule. If you miss a bedtime dose and you take only one dose daily, and you don't remember until the next morning, skip your missed dose and go back to your regular dosing schedule. Do not take 2 doses at once. Paxil Cautions If you have experienced any allergies to paroxetine or ingredients in this product, do not take this medicine and consult with your doctor. It is important that prior to taking this medicine, you have discussed your past psychiatric history with your doctor. This includes previous episodes of depression or anxiety attacks, any family members with a psychiatric disorder (e.g. bipolar disorder, depression), as well as a family history of suicide/suicide attempts. It is also important that you have discussed your past medical history with your doctor, in particular: seizures, stomach ulcers, thyroid problems, liver problems, heart problems, kidney problems, glaucoma (narrow angle type). Paxil or Paroxetine may cause you to become drowsy or dizzy, so it is advised that you refrain from driving, or operating machinery. Avoid alcohol as this will exacerbate these side effects. Please take caution if this drug is used in the elderly, as they may be more sensitive to the side effects. If the patient is taking a diuretic ("water pills"), this may interact with paroxetine to cause an electrolyte imbalance. Please consult with your doctor if you are taking these pills. If you wish to become pregnant, please discuss this with your doctor. Paroxetine should not be taken during the first three months or last three months of pregnancy. Taking paroxetine during the first three months has an association with fetal heart defects and other serious abnormalities. Babies born to mothers who have taken paroxetine during the last three months may infrequently develop symptoms including seizures, muscle stiffness, feeding/breathing difficulties, jitteriness or constant crying. If you notice any such symptoms in your new born, consult a doctor immediately. Paroxetine passes into breast milk, and due to the potential risks to the infant, it is advised that you do not breast feed while taking this medication. Paxil Side Effects Paroxetine is associated with some minor side effects that usually subside with treatment. These include weakness, nervousness, fatigue, drowsiness, nausea, vomiting, diarrhea, loss of appetite, dry mouth, sweating, dizziness, lightheadedness, or changes in sexual function. See your doctor if these symptoms continue, or if they are distressing for you. There are different types of anti depressants that differ in their potential side effects. If the disadvantages of this medicine outweigh the advantages, there may be another antidepressant more suited for you. Please discuss this with your doctor. Please see your doctor immediately if you experience any of the following: difficulty sleeping, seizures, unusual bleeding or bruising, anxiety, severe nervousness, agitation, panic attacks, feelings of irritability or hostility, impulsive behavior or other unusual changes in behavior, severe restlessness, worsening feelings of depression, thoughts of hurting yourself, or any other mental or mood changes. For men: If you experience a prolonged, painful erection, stop using this medicine and seek immediate medical attention or permanent problems could occur. Although it is unlikely to occur, please be aware of the signs of an allergic reaction. If you experience any of the following, please seek immediate medical attention: difficulty breathing, dizziness, rash, itching, or swelling of the face/throat. If you notice other effects not listed above, contact your doctor, nurse, or pharmacist. Purchase brand Paxil or generic Paroxetine at heavily discounted rates from our online pharmacy.','url':'https://www.planetdrugsdirect.com/drugs/paxil','og_descr':'Save money when safely buying Paxil online. PlanetDrugsDirect is a safe and secure Canadian international prescription referral service. Save money when safely buying Paxil online. PlanetDrugsDirect is a safe and secure Canadian international prescription referral service.Learn about the prescription medication Paxil Paroxetine Hydrochloride, drug uses, dosage, side effects, drug interactions, warnings, reviews and patient labeling. Buy Paxil Prescriptions Online at the lowest price guaranteed at CanadianPharmacyMeds.com. Description Paroxetine belongs to a class of drugs known as selective serotonin reuptake inhibitor (SSRI) antidepressants and is used to treat mental depression, obsessive-compulsive disorder (OCD), panic disorder, generalized anxiety disorder (GAD), social anxiety disorder (also known as social phobia), premenstrual dysphoric disorder (PMDD), and post-traumatic stress disorder (PTSD). SSRI-type drugs, such as it, may work by increasing the activity of the chemical serotonin in the brain. Order Paxil Prescription Medication Online for the treatment of Depression at the Lowest Price Guaranteed from CanadaDrugPharmacy.com. Can i buy clomid over the counter. Reviews about paxil for pre ejaculation. Lunesta without prescription. Natural female viagra. Paxil is the brand name for paroxetine. It’s a strong SSRI antidepressants that some doctors prescribe for premature ejaculation. Like other SSRI antidepressants, it works by adjusting the levels of serotonin in the brain. Serotonin is a chemical that carries messages between brain cells. In men who suffer from premature ejaculation, the serotonin seems to be less active in the section of the brain that controls the ejaculation. AUA Guideline on Premature Ejaculation. On a consensus of expert opinion following review of the of premature ejaculation with paroxetine. Premature Ejaculation How effective is Paxil for Premature ejaculation. Summary: This is a review of how effective Paxil paroxetine hydrochloride. May 29, 2002 Viagra, Paxil Help Premature Ejaculation. Paxil helps premature ejaculators who have not improved with standard treatment. If a man can work up the. Paxil and Premature Ejaculation. Delayed ejaculation is a well known side effect of paroxetine. Reviews. Paxil reviews for anxiety on Drugs.com;. Here s what you need to know about using Paxil for premature ejaculation Paxil is the brand Prozac for Premature reviews, premature ejaculation. The three major forms of male sexual dysfunction are ejaculatory dysfunction, erectile dysfunction (ED), and decreased libido (hypoactive sexual desire disorder). While survey findings vary considerably, most epidemiological studies suggest that premature ejaculation (PE) (Although the terms early ejaculation and rapid ejaculation recently have been suggested as more accurate descriptions of this disorder, to prevent confusion ... This is a true story of an individual who suffered from premature ejaculation. User comment s : Paroxetine helped reduce my anxiety and cases of self sabotage. Reviews about paxil for pre ejaculation Ciacil, Buy sildenafil citrate tablets 100mg. Bupropiononline. Overnight online anitbiotics. Reviews about paxil for pre ejaculation Accutane gel. Alli available uk. How To Use Paxil for Premature Ejaculation Paxil No Script Fedex Paxil With Free Dr Consultationqoo on PureVolume Our Online Pharmacy offer cheap generic Paxil with no script needed. 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In order to use Medscape, your browser must be set to accept cookies delivered by the Medscape site. To find out how to adjust your browser settings to accept cookies, please click here. Medscape uses cookies to customize the site based on the information we collect at registration. The cookies contain no personally identifiable information and have no effect once you leave the Medscape site. You can read more about our use of cookies in our privacy policy. Nov 29, 2015 Learn about indications, dosage and how it is supplied for the drug Viibryd Vilazodone Hydrochloride. Paxil CR (paroxetine hydrochloride) is an orally administered psychotropic drug with a chemical structure unrelated to other selective serotonin reuptake inhibitors or to tricyclic, tetracyclic, or other available antidepressant or antipanic agents. It is the hydrochloride salt of a phenylpiperidine compound identified chemically as (-)-trans-4R-(4'-fluorophenyl)-3S-[(3',4'-methylenedioxyphenoxy) methyl] piperidine hydrochloride hemihydrate and has the empirical formula of C19H20FNO3•HCl•1/2H2O. The molecular weight is 374.8 (329.4 as free base). The structural formula of paroxetine hydrochloride is: Pharmacokinetics Paroxetine hydrochloride is completely absorbed after oral dosing of a solution of the hydrochloride salt. The elimination half-life is approximately 15 to 20 hours after a single dose of Paxil CR. Paroxetine is extensively metabolized and the metabolites are considered to be inactive. Nonlinearity in pharmacokinetics is observed with increasing doses. Paroxetine metabolism is mediated in part by CYP2D6, and the metabolites are primarily excreted in the urine and to some extent in the feces. Pharmacokinetic behavior of paroxetine has not been evaluated in subjects who are deficient in CYP2D6 (poor metabolizers). Paroxetine hydrochloride is completely absorbed after oral dosing of a solution of the hydrochloride salt. In a study in which normal male and female subjects (n = 23) received single oral doses of Paxil CR at 4 dosage strengths (12.5 mg, 25 mg, 37.5 mg, and 50 mg), paroxetine Cmax and AUC0-inf increased disproportionately with dose (as seen also with immediate-release formulations). Mean Cmax and AUC0-inf values at these doses were 2.0, 5.5, 9.0, and 12.5 ng/mL, and 121, 261, 338, and 540 ng•hr./mL, respectively. Tmax was observed typically between 6 and 10 hours post-dose, reflecting a reduction in absorption rate compared with immediate-release formulations. The bioavailability of 25 mg Paxil CR is not affected by food. Paroxetine distributes throughout the body, including the CNS, with only 1% remaining in the plasma. Approximately 95% and 93% of paroxetine is bound to plasma protein at 100 ng/mL and 400 ng/mL, respectively. Under clinical conditions, paroxetine concentrations would normally be less than 400 ng/mL. Paroxetine does not alter the in vitro protein binding of phenytoin or warfarin. Based on studies using immediate-release formulations, steady-state drug exposure based on AUC0-24 was several-fold greater than would have been predicted from single-dose data. The excess accumulation is a consequence of the fact that 1 of the enzymes that metabolizes paroxetine is readily saturable. In steady-state dose proportionality studies involving elderly and nonelderly patients, at doses of the immediate-release formulation of 20 mg to 40 mg daily for the elderly and 20 mg to 50 mg daily for the nonelderly, some nonlinearity was observed in both populations, again reflecting a saturable metabolic pathway. In comparison to Cmin values after 20 mg daily, values after 40 mg daily were only about 2 to 3 times greater than doubled. Paroxetine is extensively metabolized after oral administration. The principal metabolites are polar and conjugated products of oxidation and methylation, which are readily cleared. Conjugates with glucuronic acid and sulfate predominate, and major metabolites have been isolated and identified. Data indicate that the metabolites have no more than 1/50 the potency of the parent compound at inhibiting serotonin uptake. The metabolism of paroxetine is accomplished in part by CYP2D6. Saturation of this enzyme at clinical doses appears to account for the nonlinearity of paroxetine kinetics with increasing dose and increasing duration of treatment. The role of this enzyme in paroxetine metabolism also suggests potential drug-drug interactions (see PRECAUTIONS: Drugs Metabolized by CYP2D6). Approximately 64% of a 30-mg oral solution dose of paroxetine was excreted in the urine with 2% as the parent compound and 62% as metabolites over a 10-day post-dosing period. About 36% was excreted in the feces (probably via the bile), mostly as metabolites and less than 1% as the parent compound over the 10-day post-dosing period. For all 3 studies, the mean dose of Paxil CR for completers at endpoint was approximately 50 mg/day. Subgroup analyses did not indicate that there were any differences in treatment outcomes as a function of age or gender. Long-term maintenance effects of the immediate-release formulation of paroxetine in panic disorder were demonstrated in an extension study. Patients who were responders during a 10-week double-blind phase with immediate-release paroxetine and during a 3-month double-blind extension phase were randomized to either immediate-release paroxetine or placebo in a 3-month double-blind relapse prevention phase. Patients randomized to paroxetine were significantly less likely to relapse than comparably treated patients who were randomized to placebo. In a third study employing intermittent dosing, patients (N = 366) were treated for the 2 weeks prior to the onset of menses (luteal phase dosing, also known as intermittent dosing) with 12.5 mg/day or 25 mg/day of PAXIL CR or placebo for a period of 3 months. 12.5 mg/day and 25 mg/day of PAXIL CR, as luteal phase dosing, was significantly more effective than placebo as measured by change from baseline luteal phase VAS total score. There is insufficient information to determine the effect of race or age on outcome in these studies. Starting Paxil CR in a patient who is being treated with MAOIs such as linezolid or intravenous methylene blue is also contraindicated because of an increased risk of serotonin syndrome (see WARNINGS and DOSAGE AND ADMINISTRATION). Concomitant use with thioridazine is contraindicated (see WARNINGS and PRECAUTIONS). Concomitant use in patients taking pimozide is contraindicated (see PRECAUTIONS). Paxil CR is contraindicated in patients with a hypersensitivity to paroxetine or to any of the inactive ingredients in Paxil CR. Clinical Worsening and Suicide Risk Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications, and this risk may persist until significant remission occurs. Suicide is a known risk of depression and certain other psychiatric disorders, and these disorders themselves are the strongest predictors of suicide. There has been a long-standing concern, however, that antidepressants may have a role in inducing worsening of depression and the emergence of suicidality in certain patients during the early phases of treatment. Pooled analyses of short-term placebo-controlled trials of antidepressant drugs (SSRIs and others) showed that these drugs increase the risk of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults (ages 18-24) with major depressive disorder (MDD) and other psychiatric disorders. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24; there was a reduction with antidepressants compared to placebo in adults aged 65 and older. The pooled analyses of placebo-controlled trials in children and adolescents with MDD, obsessive compulsive disorder (OCD), or other psychiatric disorders included a total of 24 short-term trials of 9 antidepressant drugs in over 4,400 patients. The pooled analyses of placebo-controlled trials in adults with MDD or other psychiatric disorders included a total of 295 short-term trials (median duration of 2 months) of 11 antidepressant drugs in over 77,000 patients. There was considerable variation in risk of suicidality among drugs, but a tendency toward an increase in the younger patients for almost all drugs studied. There were differences in absolute risk of suicidality across the different indications, with the highest incidence in MDD. The risk differences (drug vs placebo), however, were relatively stable within age strata and across indications. These risk differences (drug-placebo difference in the number of cases of suicidality per 1,000 patients treated) are provided in Table 1. Serotonin syndrome symptoms may include mental status changes (e.g., agitation, hallucinations, delirium, and coma), autonomic instability (e.g., tachycardia, labile blood pressure, dizziness, diaphoresis, flushing, hyperthermia), neuromuscular symptoms (e.g., tremor, rigidity, myoclonus, hyperreflexia, incoordination), seizures, and/or gastrointestinal symptoms (e.g., nausea, vomiting, diarrhea). Patients should be monitored for the emergence of serotonin syndrome. The concomitant use of Paxil CR with MAOIs intended to treat psychiatric disorders is contraindicated. Paxil CR should also not be started in a patient who is being treated with MAOIs such as linezolid or intravenous methylene blue. All reports with methylene blue that provided information on the route of administration involved intravenous administration in the dose range of 1 mg/kg to 8 mg/kg. No reports involved the administration of methylene blue by other routes (such as oral tablets or local tissue injection) or at lower doses. There may be circumstances when it is necessary to initiate treatment with an MAOI such as linezolid or intravenous methylene blue in a patient taking Paxil CR. Paxil CR should be discontinued before initiating treatment with the MAOI (see CONTRAINDICATIONS and DOSAGE AND ADMINISTRATION). If concomitant use of Paxil CR with certain other serotonergic drugs, i.e., triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, buspirone, tryptophan, and St. John’s Wort is clinically warranted, be aware of a potential increased risk for serotonin syndrome, particularly during treatment initiation and dose increases. Treatment with Paxil CR and any concomitant serotonergic agents should be discontinued immediately if the above events occur and supportive symptomatic treatment should be initiated. Infants exposed to SSRIs in pregnancy may have an increased risk for persistent pulmonary hypertension of the newborn (PPHN). PPHN occurs in 1 – 2 per 1,000 live births in the general population and is associated with substantial neonatal morbidity and mortality. Several recent epidemiologic studies suggest a positive statistical association between SSRI use (including Paxil CR) in pregnancy and PPHN. Other studies do not show a significant statistical association. Physicians should also note the results of a prospective longitudinal study of 201 pregnant women with a history of major depression, who were either on antidepressants or had received antidepressants less than 12 weeks prior to their last menstrual period, and were in remission. Women who discontinued antidepressant medication during pregnancy showed a significant increase in relapse of their major depression compared to those women who remained on antidepressant medication throughout pregnancy. When treating a pregnant woman with Paxil CR, the physician should carefully consider both the potential risks of taking an SSRI, along with the established benefits of treating depression with an antidepressant. This decision can only be made on a case by case basis (see DOSAGE AND ADMINISTRATION and ADVERSE REACTIONS, Postmarketing Reports). The steady-state pharmacokinetics of paroxetine was not altered when administered with digoxin at steady state. Mean digoxin AUC at steady state decreased by 15% in the presence of paroxetine. Since there is little clinical experience, the concurrent administration of Paxil CR and digoxin should be undertaken with caution. Ten percent (21/212) of patients treated with Paxil CR discontinued treatment due to an adverse event in a pool of 2 studies of patients with major depressive disorder. The most common events (≥1%) associated with discontinuation and considered to be drug related (i.e., those events associated with dropout at a rate approximately twice or greater for Paxil CR compared to placebo) included the following: The most commonly observed adverse events associated with the use of Paxil CR either during continuous dosing or luteal phase dosing (incidence of 5% or greater and incidence for Paxil CR at least twice that for placebo, derived from Table 6) 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 2 enumerates adverse events that occurred at an incidence of 1% or more among patients treated with Paxil CR, aged 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 3 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 4 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 5 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 patients were dosed in a range of 12.5 to 37.5 mg/day. Table 6 enumerates adverse events that occurred at an incidence of 1% or more among patients treated with Paxil CR who participated in three, 12-week, placebo-controlled trials in PMDD in which patients were dosed at 12.5 mg/day or 25 mg/day and in one 12-week placebo-controlled trial in which patients were dosed for 2 weeks prior to the onset of menses (luteal phase dosing) at 12.5 mg/day or 25 mg/day. Reported adverse events were classified using a standard COSTART-based Dictionary terminology. The prescriber should be aware that these figures cannot be used to predict the incidence of side effects in the course of usual medical practice where patient characteristics and other factors differ from those that prevailed in the clinical trials. Similarly, the cited frequencies cannot be compared with figures obtained from other clinical investigations involving different treatments, uses, and investigators. The cited figures, however, do provide the prescribing physician with some basis for estimating the relative contribution of drug and nondrug factors to the side effect incidence rate in the population studied. a. Adverse events for which the Paxil CR reporting incidence was less than or equal to the placebo incidence are not included. These events are nausea and respiratory disorder. b. <1% means greater than zero and less than 1 %. c. Based on the number of males. d. Mostly anorgasmia or delayed ejaculation. Significant weight loss may be an undesirable result of treatment with paroxetine for some patients but, on average, patients in controlled trials with Paxil CR or the immediate-release formulation, had minimal weight loss (about 1 pound). No significant changes in vital signs (systolic and diastolic blood pressure, pulse, and temperature) were observed in patients treated with Paxil CR, or immediate-release paroxetine hydrochloride, in controlled clinical trials. In a study of elderly patients with major depressive disorder, 3 of 104 patients treated with Paxil CR and none of 109 placebo patients experienced liver transaminase elevations of potential clinical concern. Two of the patients treated with PAXIL CR dropped out of the study due to abnormal liver function tests; the third patient experienced normalization of transaminase levels with continued treatment. Also, in the pool of 3 studies of patients with panic disorder, 4 of 444 patients treated with PAXIL CR and none of 445 placebo patients experienced liver transaminase elevations of potential clinical concern. Elevations in all 4 patients decreased substantially after discontinuation of PAXIL CR. The clinical significance of these findings is unknown. In placebo-controlled clinical trials with the immediate-release formulation of paroxetine, patients exhibited abnormal values on liver function tests at no greater rate than that seen in placebo-treated patients. Paxil CR® (PAX-il) (paroxetine hydrochloride) Controlled-Release Tablets Read the Medication Guide that comes with Paxil CR before you start taking it and each time you get a refill. There may be new information. This Medication Guide does not take the place of talking to your healthcare provider about your medical condition or treatment. Talk with your healthcare provider if there is something you do not understand or want to learn more about. What is the most important information I should know about Paxil CR? Paxil CR and other antidepressant medicines may cause serious side effects, including: 1. Suicidal thoughts or actions: 5. Abnormal bleeding: Paxil CR and other antidepressant medicines may increase your risk of bleeding or bruising, especially if you take the blood thinner warfarin (Coumadin®, Jantoven®), a non-steroidal anti-inflammatory drug (NSAIDs, like ibuprofen or naproxen), or aspirin. 6. Seizures or convulsions 7. Manic episodes: What is Paxil CR? Paxil CR is a prescription medicine used to treat depression. It is important to talk with your healthcare provider about the risks of treating depression and also the risks of not treating it. You should discuss all treatment choices with your healthcare provider. Paxil CR is also used to treat: ∘ Do not take an MAOI within 2 weeks of stopping Paxil CR unless directed to do so by your physician. ∘ Do not start Paxil CR if you stopped taking an MAOI in the last 2 weeks unless directed to do so by your physician. ∘ People who take Paxil CR close in time to an MAOI may have serious or even life-threatening side effects. Get medical help right away if you have any of these symptoms: What should I avoid while taking Paxil CR? Paxil CR can cause sleepiness or may affect your ability to make decisions, think clearly, or react quickly. You should not drive, operate heavy machinery, or do other dangerous activities until you know how Paxil CR affects you. Do not drink alcohol while using Paxil CR. What are possible side effects of Paxil CR? Paxil CR may cause serious side effects, including all of those described in the section entitled “What is the most important information I should know about Paxil CR? ” Common possible side effects in people who take Paxil CR include: Tell your healthcare provider if you have any side effect that bothers you or that does not go away. These are not all the possible side effects of Paxil CR. For more information, ask your healthcare provider or pharmacist. CALL YOUR DOCTOR FOR MEDICAL ADVICE ABOUT SIDE EFFECTS. YOU MAY REPORT SIDE EFFECTS TO THE FDA AT 1-800-FDA-1088 or 1-800-332-1088. How should I store Paxil CR?','url':'http://www.drugs.com/pro/paxil-cr.html','og_descr':'Paxil CR official prescribing information for healthcare professionals. Includes: indications, dosage, adverse reactions, pharmacology and more.
Nov 28, 2015 Learn about indications, dosage and how it is supplied for the drug Luvox Fluvoxamine Maleate Tablets. Drug information on Paxil, Paxil CR, Pexeva (paroxetine), includes drug pictures, side effects, drug interactions, directions for use, symptoms of overdose, and what to avoid.
Medscape - Depression-specific dosing for Paxil, Paxil CR paroxetine, frequency-based adverse effects, target dose 40 mg/day, not to exceed 60 mg/day, OR. Find a comprehensive guide to possible side effects when taking Paxil (Paroxetine Hydrochloride) for Professionals, Patients, and Caregivers. Find patient medical information for paroxetine oral on WebMD including its uses, side effects and safety, interactions, pictures, warnings and user ratings.PAROXETINE - paroxetine hydrochloride tablet, film coated Teva Pharmaceuticals USA-----PAROXETINE TABLETS USP, 10 mg, 20 mg, 30 mg and 40 mg. |