Effexor XR - MAIN AND GENERAL FORUM - HPPD Support. Dear Drugs-Forum readers: We are a small non-profit that runs one of the most read drug information & addiction help websites in the world. If everyone reading this would donate then this fund raiser would be done in an hour. I had depression, social anxiety and negative symptoms of schizophrenia. Thanks again for sharing your experience I've been offered effexor several times and turned it down everytime. Hes thinking about prescribing Effexor XR since that supposedly deals with the anxiety siide making it easier to cope with the DR. Mht tell him about keppra, im still kinda undecided about whether i should go on meds.
The History of Hypnosis I just got it filled today and will be starting it to. "Once upon a time, there was a boy who lived in a house across the field, from a girl who no longer exists. I know it can cause stomach upset and I am fairly sensitive to that..wondering if anyone else out there is on it or has tried it? I was instructed to take the med with my largest meal to avoid any nausea. I did feel like I was "almost" going to get diarrhea the first couple of days, but did not. Learn about the history of hypnosis starting from the work of Mesmer, 19th Centruy, James Braid, and modern day hypnosis.
Effexor venlafaxine SNRI - Social Anxiety Forum A friend of mine came off it at the same time, and she switched to fluoxetine for about a month I think (is that rht nzmum? Drugs Paxil, Zoloft, Wellbutrin, Effexor XR, Xanax, Propanolol. I was on Effexor XR 150mg for about 2 years before recently stopping.
Effexor XR - Depression Message Board - HealthBoards A gradual yet shocking decrease in my memory: word retrieval, short term memory, sense of ‘fuzziness’ about events in recent past. I changed from Effexor to Effexor XR a few weeks ago. I moved from taking it at nht to taking it in the morning because I get withdrawal syoms before my nextADDED the effexor and started feeling better in 6 weeks. i am sick of seeing all these negative comments about effexor on all these message boards. of course.
Lexapro does work! Give it a chance. - We serve over 3 million readers per month, and have costs like all popular websites: servers, hosting, licenses and software. If Drugs-Forum is useful to you, take one minute to keep it online another year by donating whatever you can today. I was at the university but couldn't go to classes because of these. I've tried just about every SSRI but never an SNRI (effexor, cymbalta) because I'm afraid of the side effects. The SSRIs don't do much I don't think for my anxiety (1 mg clonazepam x3/day helps a lot) but I stay depressed. I recently began taking Lexapro. 4 weeks ago. I suffered from depression for years and would never think of taking a drug for it, but finally I'd come to.
Effexor XR oral Uses, Side Effects, Interactions, Pictures. I know it can cause stomach upset and I am fairly sensitive to that..wondering if anyone else out there is on it or has tried it? Now, I have constipation, so am trying to eat more fiber to get that under control. This is the easiest AD I have ever started on, and so far I am really happy with it. Find patient medical information for Effexor XR oral on WebMD including its uses, side effects and safety, interactions, pictures, warnings and user ratings. Message Boards. Connect with people like you, and get expert guidance on living a healthy life.
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Paxil CR or Effexor XR. - Depression Message Board Immediate release 25-50 mg/day PO divided q8-12hr initially; may be increased as tolerated by ≤25 mg/day no faster than every 4 days Moderate: Up to 225 mg/day PO divided q8-12hr Severe: Up to 375 mg/day PO divided q8-12hr Extended release 37.5 mg PO once daily initially; may be increased by 37.5 mg/day every 4-7 days; not to exceed 225 mg/day Headache (25-38%) Nausea (21-58%) Insomnia (15-24%) Asthenia (16-20%) Dizziness (11-24%) Ejaculation disorder (2-19%) Somnolence (12-26%) Dry mouth (12-22%) Diaphoresis (7-19%) Anorexia (15-17%) Nervousness (17-26%) Anorgasmia (5-13%) Weht loss (1-6%) Abnormal vision (4-6%) Hypertension (2-5%) Impotence (4-6%) Paresthesia (2-3%) Tremor (1-10%) Vasodilation (2-6%) Vomiting (3-8%) Weht gain (2%) Flatulence (3-4%) Pruritus (1%) Yawning (3-8%) Dyspepsia (5-7%) Twitching (1-3%) Mydriasis (2%) 65 years Not FDA approved for children; in children and young adults; benefits of taking antidepressants must be wehed against risks Patients should be monitored closely for changes in behavior, clinical worsening, and suicidal tendencies; this should be done during initial 1-2 months of therapy and dosage adjustments Patient’s family should communicate any abrupt behavioral changes to healthcare provider Worsening behavior and suicidal tendencies that are not part of presenting symptoms may necessitate discontinuance of therapy Not FDA approved for treatment of bipolar depression Risk of mydriasis; may trger angle closure attack in patients with angle closure glaucoma with anatomiy narrow angles without a patent iridectomy Use caution in bipolar mania, history of seizures, and cardiovascular disease May precipitate mania or hypomania episodes in patients with bipolar disorder; avoid monotherapy in bipolar disorder; screen patients presenting with depressive symptoms for bipolar disorder Use caution in hepatic or renal impairment Neonates exposed to serotonin-norepinephrine reuptake inhibitors (SNRIs) or selective serotonin reuptake inhibitors (SSRIs) late in 3rd trimester of pregnancy have developed complications necessitating prolonged hospitalization, respiratory support, and tube feeding Clinical worsening and suicidal ideation may occur despite medication in adolescents and young adults (18-24 years) When discontinuing, taper dosage to avoid flulike symptoms May cause increase in nervousness, anxiety, or insomnia May impair ability to operate heavy machinery; depresses CNS Bone fractures reported with antidepressant therapy; consider possibility if patient experiences bone pain May cause snificant increase in serum cholesterol Dose-dependent anorectic effects and weht loss reported in children and adult patients Dose-related increase in systolic and diastolic pressure reported Eosinophilic pneumonia and interstitial lung disease reported SAIDH and hyponatremia reported SSRIs Potentially life-threatening serotonin syndrome with SSRIs and SNRIs when used in combination with other serotonergic agents including TCAs, buspirone tryptophan, fentanyl, tramadol, lithium, and triptans; symptoms include tremor, myoclonus, diaphoresis, nausea, vomiting, flushing, dizziness, hyperthermia with features resembling neuroleptic malnant syndrome, seizures, ridity, autonomic instability with possible rapid fluctuations of vital sns, and mental status changes that include extreme agitation progressing to delirium and coma Venlafaxine in patient being treated with linezolid or IV methylene blue increases risk of serotonin syndrome; if linezolid or IV methylene blue must be administered, discontinue venlafaxine immediately and monitor for central nervous system (CNS) toxicity; therapy may be resumed 24 hours after last linezolid or methylene blue dose or after 2 weeks of monitoring, whichever comes first SSRIs and SNRIs may impair platelet aggregation and increase the risk of bleeding events, ranging from ecchymoses, hematomas, epistaxis, petechiae, and GI hemorrhage to life-threatening hemorrhage; concomitant use of aspirin, NSAIDs, warfarin, other anticoagulants, or other drugs known to affect platelet function may add to this risk Control hypertension before initiating treatment; monitor blood pressure regularly during treatment Risks of sustained hypertension, hyponatremia, and impeded heht and weht in children Drug-laboratory test interactions: False-positive urine immunoassay screening tests for phencyclidine (PCP) and amphetamine have been observed during venlafaxine therapy because of lack of specificity of the screening tests May cause or exacerbate sexual dysfunction "Bicyclic" antidepressant; drug is structurally unrelated to SSRIs, MAOIs, and tricyclic antidepressants (TCAs), but it and its metabolite are potent inhibitors of serotonin and norepinephrine reuptake and weak inhibitors of dopamine reuptake; it does not have MAOI activity or activity for H1 histaminergic, muscarinic cholinergic, or alpha2-adrenergic receptors The above information is provided for general informational and educational purposes only. Despite what you see on the boards.the negative stuff.people have been helped by antidepressants long term. Effexor XR has worked the best in that it "lifted" the major part, but still mildly depressed.
Effexor XR Forum Antidepressant medications are used to treat a variety of conditions, including depression and other mental/mood disorders. This has little to do with the saxophone, but I'm posting this on every message board I freqent because I think it's important.i find this thread very interesting as i have a friend who is struggling with her life who is on Effexor XR®. she indicated that she needs it but i got the feeling from the.