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    CCHBs are bilingual/bicultural health workers who bridge language and cultural barriers. They work with patients from their communities to access medical and social services and to empower them to make informed decisions. They support the relationship between patients and family doctors. Our consultation clinic sees patients who self-identify as experiencing cultural and language barriers to accessing health care and have a referral from a family physician. A consultation clinic works with the patient’s family physician to provide specialized diagnostic and management support. Currently our clinic is staffed by Middle Eastern (Arabic-speaking), Iranian/Afghan (Farsi/Pashto/Dari-speaking), Latin American (Spanish-speaking), and Eritrean (Tigrinya/Amharic-speaking) Cross Cultural Health Brokers. clomid 3-7 Tamoxifen belongs to the group of cancer-fighting medications known as antineoplastics, and specifically to the type of antineoplastics known as antiestrogens. It is used in combination with other medications to treat early breast cancer. Tamoxifen fights certain types of breast cancer, called hormone responsive or estrogen receptor positive breast cancer, by blocking the effects of the hormone estrogen in the body. This prevents the growth of the types of breast cancer cells that require estrogen for growth and survival. It is also used to treat breast cancer that is advanced or has spread to other parts of the body. This medication may be available under multiple brand names and/or in several different forms. Any specific brand name of this medication may not be available in all of the forms or approved for all of the conditions discussed here.

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    Tamoxifen is used to treat breast cancer that has spread to other parts of the body metastatic breast cancer, to treat. Common Brand Names Nolvadex. buy xenical weight loss pills Note the absence of estrogen name receptors in breast cancer brand cells does not necessarily mean that tamoxifen tamoxifen side effects will be name. Learn about Nolvadex Tamoxifen Citrate may treat, uses, dosage, side effects, drug interactions. Generic Name tamoxifen citrate; Brand Name Nolvadex.

    Generic name: Tamoxifen uses generic names in all descriptions of drugs. In some cases, health care professionals may use the trade name Nolvadex when referring to the generic drug name Tamoxifen. This medication is classified as an "anti-estrogen." (For more detail, see "How this drug works" section below). side effect of tamoxifen is blood clots, including deep vein thrombosis (DVT) and pulmonary embolus. You should seek emergency help and notify your health care provider immediately if you develop sudden chest pain and shortness of breath. Notify your health care provider within 24 hours if you notice that one leg is swollen, red, painful and/or warm to touch and the other is not. A side effect of tamoxifen can be the development of uterine cancer. Women who have not had a hysterectomy should have regular pap smears and gyn examinations. Abnormal vaginal bleeding should be reported to your health care provider. Generic drugs usually cost less than a brand-name drug. Tamoxifen oral tablet is only available as a generic drug. Tamoxifen is used to treat and reduce the risk of certain types of breast cancer. Tamoxifen belongs to a group of drugs called antiestrogens. A class of drugs is a group of medications that work in a similar way. These drugs are often used to treat similar conditions. Antiestrogens work by blocking the effects of the hormone estrogen in the body.

    Tamoxifen brand name

    Tamoxifen Oral Route Description and Brand Names - Mayo Clinic, Brand name tamoxifen! Tamoxifen non prescription ~ Pediatric.

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  5. Tamoxifen, sold under the brand name Nolvadex among others, is a medication that is used to prevent breast cancer in women and treat breast cancer in.

    • Tamoxifen - Wikipedia
    • Nolvadex Tamoxifen Citrate Side Effects, Interactions, Warning.
    • Tamoxifen Nolvadex - Side Effects, Dosage, Interactions - Drugs

    BRAND NAMES Nolvadex, Soltamox. Warning Medication Uses How To Use Side Effects Precautions Drug Interactions Overdose Notes Missed. viagra for men tablets Find patient medical information for Tamoxifen Oral on WebMD including its uses. COMMON BRANDS Nolvadex, Soltamox. GENERIC NAMES Tamoxifen. Tamoxifen Sandoz Tablets is a brand of medicine containing the active. Brand name Tamoxifen Sandoz Tablets; Active ingredient Tamoxifen; Schedule S4.

     
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    Day 1: 8 mg PO before breakfast, 4 mg after lunch and after dinner, and 8 mg at bedtime Day 2: 4 mg PO before breakfast, after lunch, and after dinner and 8 mg at bedtime Day 3: 4 mg PO before breakfast, after lunch, after dinner, and at bedtime Day 4: 4 mg PO before breakfast, after lunch, and at bedtime Day 5: 4 mg PO before breakfast and at bedtime Day 6: 4 mg PO before breakfast May be tapered over 12 days (to decrease chance of dermatitis flareup) Methylprednisolone: Usual dosing range, 2-60 mg/day PO divided q6-24hr Methylprednisolone acetate: Usual dosing range, 10-80 mg IM every 1-2 weeks; as temporary substitute for PO, given in daily IM dose equal to daily PO dose; for prolonged effect, given in weekly IM dose equal to 7 times daily PO dose; unlike methylprednisolone sodium succinate, may not be given IV Methylprednisolone sodium succinate: Usual dosing range, 10-250 mg IM/IV up to q4hr PRN Acne Adrenal suppression Amenorrhea Delayed wound healing Delirium Diabetes mellitus Edema Emotional instability Erythema Fluid retention GI perforation Glucose intolerance Growth suppression (children) Hallucinations Headache Hepatomegaly Hepatitis Hypokalemic alkalosis Increased transaminases Insomnia Leukocytosis Menstrual irregularity Myopathy Neuritis Osteoporosis Peptic ulcer Perianal pruritus Pituitary adrenal axis suppression Protein catabolism Pseudotumor cerebri (on withdrawal) Psychosis Sodium and water retention Seizure Tachycardia Ulcerative esophagitis Urticaria Vasculitis Vertigo Weight gain Untreated serious infections Documented hypersensitivity to drug or components (eg, lactose monohydrate from cow milk) Intrathecal administration Systemic fungal infection (except intra-articular injection in localized joint conditions) IM route is contraindicated in idiopathic thrombocytopenic purpura Premature infants (formulations containing benzyl alcohol only) Traumatic brain injury (high doses) Administration of live or live, attenuated vaccines is contraindicated in patients receiving immunosuppressive doses of corticosteroids Use with caution in cirrhosis, ocular herpes simplex, hypertension, diverticulitis, hypothyroidism, myasthenia gravis, peptic ulcer disease, osteoporosis, ulcerative colitis, psychotic tendencies, renal insufficiency, pregnancy, diabetes mellitus, history of seizure disorders, multiple sclerosis, thromboembolic disorders, myocardial infarction Long-term treatment: Risk of osteoporosis, myopathy, delayed wound healing Minimal mineralocorticoid activity Use in septic shock or sepsis syndrome not proven effective and may increase mortality in some patients including patients with elevated serum creatinine and patients who develop secondary infections Clearance of corticosteroids may increase in hyperthyroid patients and decrease in hypothyroid ones; dose adjustments may be necessary Patients receiving corticosteroids should avoid chickenpox or measles-infected persons if unvaccinated Latent tuberculosis may be reactivated (patients with positive tuberculin test should be monitored) Some suggestion (not fully substantiated) of slightly increased cleft palate risk if corticosteroids are used in pregnancy May cause hypothalamic-pituitary-adrenal (HPA) axis suppression, Cushing syndrome, or hyperglycemia Prolonged corticosteroid use may result in elevated IOP, glaucoma, or cataracts Killed or inactivated vaccines may be administered; however, the response to such vaccines cannot be predicted Immunization procedures may be undertaken in patients who are receiving corticosteroids as replacement therapy in physiologic doses (eg, for Addison’s disease) Injection may result in dermal and/or subdermal changes forming depressions in the skin at injection site; to minimize incidence of dermal and subdermal atrophy, care must be exercised not to exceed recommended doses in injections; avoid injection into deltoid muscle due to high incidence of subcutaneous atrophy Increased dosage of rapidly acting corticosteroids indicated in patients on corticosteroid therapy subjected to any unusual stress before, during, and after the stressful situation Not for use in the treatment of traumatic brain injury Average and large doses of corticosteroids can cause elevation of blood pressure, salt and water retention, and increased excretion of potassium; dietary salt restriction and potassium supplementation may be necessary; all corticosteroids increase calcium excretion Drug induced secondary adrenocortical insufficiency may be minimized by gradual reduction of dosage; relative insufficiency may persist for months after discontinuation of therapy; therefore, in situation of stress occurring during that period, hormone therapy should be reinstituted Rarely, high doses of cyclically pulsed intravenous methylprednisolone (usually for the treatment of exacerbations of multiple sclerosis at doses of 1 g/day) can induce a toxic form of acute hepatitis; discontinue therapy if it occurs; since recurrence has occurred after re-challenge, avoid use in patients with a history of toxic hepatitis caused by methylprednisolone With increasing doses of corticosteroids, the rate of occurrence of infectious complications increases; corticosteroids may also mask some signs of current infection; corticosteroids may exacerbate systemic fungal infections and should not be used in presence of such infections unless needed to control drug reactions; latent amebiasis or active amebiasis should be ruled out before initiating corticosteroid therapy patients who have spent time in tropics or patients with unexplained diarrhea Lowest possible dose should be used to control condition under treatment; when reduction in dosage possible, reduction should be gradual Risk/benefit decision must be made in each individual case as to dose and duration of treatment and as to whether daily or intermittent therapy should be used Kaposi’s sarcoma reported in patients receiving corticosteroid therapy, most often for chronic conditions; discontinuation of therapy may result in clinical improvement Although controlled clinical trials have shown corticosteroids to be effective in speeding the resolution of acute exacerbations of multiple sclerosis, they do not affect the ultimate outcome or natural history of the disease Psychic derangements may appear when corticosteroids used, ranging from euphoria, insomnia, mood swings, personality changes, and severe depression, to frank psychotic manifestations; also, existing emotional instability or psychotic tendencies may be aggravated by corticosteroids Give consideration to potential for hypersensitivity reactions to cow’s milk ingredients in Solumedrol; if appropriate, stop administration of injection solution Solumedrol and treat patient’s condition accordingly; alternative treatments, including use of corticosteroid formulations that do not contain ingredients produced from cow’s milk, should be considered for acute allergy management Increased incidence of scleroderma reported in patients with systemic sclerosis; use caution Potent glucocorticoid with minimal to no mineralocorticoid activity Modulates carbohydrate, protein, and lipid metabolism and maintenance of fluid and electrolyte homeostasis Controls or prevents inflammation by controlling rate of protein synthesis, suppressing migration of polymorphonuclear leukocytes (PMNs) and fibroblasts, reversing capillary permeability, and stabilizing lysosomes at cellular level Solution: D5/0.5 NS, D5/NS, D5W, LR, NS Additive: Chloramphenicol sodium succinate, cimetidine, clindamycin, dopamine, granisetron, heparin, norepinephrine, penicillin G potassium, ranitidine, theophylline, verapamil Syringe: Diatrizoate meglumine, diatrizoate meglumin/diatrizoate sodium, granisetron, iohexol, iopamidol, iothalamate meglumine, ioxalate meglumine/ioxalate sodium, metoclopramide Y-site (partial list): Acyclovir, amifostine, amiodarone, cisplatin, dopamine, enalaprilat, famotidine, heparin, inamrinone, linezolid, meperidine, metronidazole, midazolam, morphine, sodium bicarbonate Additive: Aminophylline(? ), glycopyrrolate, metaraminol, nafcillin, penicillin G sodium Syringe: Doxapram Y-site: Allopurinol, amsacrine, ciprofloxacin, cisatracurium(? ), etoposide phosphate, fenoldopam, filgrastim, gemcitabine, heparin/hydrocortisone(? ), propofol, sargramostim, vinorelbine, vitamins B and C(? ) Inject directly into vein or into tubing of running IV Injection: Administer over at least 1 minute Infusion: Further dilute reconstituted mixture with D5W, NS, D5/NS, or other compatible solution Push: Administer over 10-20 minutes The above information is provided for general informational and educational purposes only. 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