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Controlled studies in pregnant women show no evidence of fetal risk. Ivim divided q4-6hr not to exceed 16 mgday plasma cortisol level then determined at 800 am on following morning level will be decreased in normal individuals but at baseline level in cushing syndrome cardiovascular bradycardia, cardiac arrest, cardiac arrhythmias, cardiac enlargement, circulatory collapse, congestive heart failure, fat embolism, hypertension, hypertrophic cardiomyopathy in premature infants, myocardial rupture following recent myocardial infarction, edema, pulmonary edema, syncope, tachycardia, thromboembolism, thrombophlebitis, vasculitis dermatologic acne, allergic dermatitis, dry scaly skin, ecchymoses and petechiae, erythema, impaired wound healing, increased sweating, rash, striae, suppression of reactions to skin tests, thin fragile skin, thinning scalp hair, urticaria endocrine decreased carbohydrate and glucose tolerance, development of cushingoid state, hyperglycemia, glycosuria, hirsutism, hypertrichosis, increased requirements for insulin or oral hypoglycemic agents in diabetes, manifestations of latent diabetes mellitus, menstrual irregularities, secondary adrenocortical and pituitary unresponsiveness (particularly in times of stress, as in trauma, surgery, or illness), suppression of growth in pediatric patients fluid and electrolyte disturbances congestive heart failure in susceptible patients, fluid retention, hypokalemic alkalosis, potassium loss, sodium retention, tumor lysis syndrome gastrointestinal abdominal distention, elevation in serum liver enzyme levels (usually reversible upon discontinuation), hepatomegaly, increased appetite, nausea, pancreatitis, peptic ulcer with possible perforation and hemorrhage, perforation of the small and large intestine (particularly in patients with inflammatory bowel disease), ulcerative esophagitis metabolic negative nitrogen balance due to protein catabolismmusculoskeletal aseptic necrosis of femoral and humeral heads, loss of muscle mass, muscle weakness, osteoporosis, pathologic fracture of long bones, steroid myopathy, tendon rupture, vertebral compression fractures neurologicalpsychiatric convulsions, depression, emotional instability, euphoria, headache, increased intracranial pressure with papilledema (pseudotumor cerebri) usually following discontinuation of treatment, insomnia, mood swings, neuritis, neuropathy, paresthesia, personality changes, psychic disorders, vertigo ophthalmic exophthalmos, glaucoma, increased intraocular pressure, posterior subcapsular cataracts, vision blurred other abnormal fat deposits, decreased resistance to infection, hiccups, increased or decreased motility and number of spermatozoa, malaise, moon face, weight gain administration of live or live, attenuated vaccines is contraindicated in patients receiving immunosuppressive doses of corticosteroids use with caution in cirrhosis, diverticulitis, myasthenia gravis, peptic ulcer disease, ulcerative colitis, renal insufficiency, pregnancy average and large doses of corticosteroids can cause elevation of blood pressure, sodium and water retention, and increased excretion of potassium these effects are less likely to occur with synthetic derivatives except when used in large doses dietary salt restriction and potassium supplementation may be necessary all corticosteroids increase calcium excretion literature reports suggest apparent association between use of corticosteroids and left ventricular free wall rupture after recent myocardial infarction therapy with corticosteroids should be used with great caution in these patients corticosteroids can produce reversible hypothalamic-pituitary adrenal (hpa) axis suppression with potential for glucocorticosteroid insufficiency after withdrawal of treatment adrenocortical insufficiency may result from too rapid withdrawal may be minimized by gradual reduction of dosage relative insufficiency may persist for months after discontinuation of therapy therefore, in any situation of stress occurring during that period, reinstitute hormone therapy if patient is receiving steroids already, may increase dosage metabolic clearance of corticosteroids is decreased in hypothyroid patients and increased in hyperthyroid patients changes in thyroid status of patient may necessitate adjustment in dosage corticosteroids may exacerbate systemic fungal infections not for use in presence of such infections unless needed to control life-threatening drug reactions concomitant use of amphotericin b and hydrocortisone followed by cardiac enlargement and congestive heart failure reported latent disease may be activated or there may be an exacerbation of intercurrent infections due to pathogens, including those caused by amoeba, candida, cryptococcus, mycobacterium, nocardia, pneumocystis, toxoplasma rule out latent amebiasis or active amebiasis before initiating corticosteroid therapy in any patient who has spent time in the tropics or any patient with unexplained diarrhea corticosteroids should be used with great care in patients with known or suspected strongyloides (threadworm) infestation corticosteroid-induced immunosuppression may lead to strongyloides hyperinfection and dissemination with widespread larval migration, often accompanied by severe enterocolitis and potentially fatal gram-negative septicemia not for use in cerebral malaria close observation necessary if corticosteroids are indicated in patients with latent tuberculosis or tuberculin reactivity reactivation of the disease may occur during prolonged corticosteroid therapy, these patients should receive chemoprophylaxis use of oral corticosteroids not recommended in treatment of optic neuritis and may lead to increase in risk of new episodes corticosteroids should not be used in active ocular herpes simplex use lowest possible dose to control condition under treatment riskbenefit 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 may lead to inhibition of bone growth in pediatric patients and development of osteoporosis at any age special consideration should be given to patients at increased risk of osteoporosis (e. Psychic derangements may appear when corticosteroids are used, ranging from euphoria, insomnia, mood swings, personality changes, and severe depression, to frank psychotic manifestations existing emotional instability or psychotic tendencies may also be aggravated by corticosteroids may have systemic and local effects examine joint fluid, as necessary to exclude a septic process avoid injection into infected site frequent intra-articular injections may result in damage to joint tissue if exposed to chickenpox, prophylaxis with varicella zoster immune globulin (vzig) may be indicated if exposed to measles, prophylaxis with immune globulin (ig) may be indicated if chickenpox develops, treatment with antiviral agents should be considered 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 prolonged corticosteroid use may result in elevated intraocular pressure, glaucoma, or cataracts with possible damage to optic nerves, and may enhance establishment of secondary ocular infections due to bacteria, fungi, or viruses consider referral to ophthalmologist for patients who develop ocular symptoms or use corticosteroid-containing products for more than 6 weeks 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 addisons disease) serious neurologic events, some resulting in death, have been reported with epidural injection specific events reported include, but are not limited to, spinal cord infarction, paraplegia, quadriplegia, cortical blindness, and stroke these serious neurologic events have been reported with and without use of fluoroscopy safety and effectiveness of epidural administration of corticosteroids have not been established, and corticosteroids are not approved for this use generally acceptable.

Iv divided q6hr for first 2-4 days of antibiotic therapy, starting 10-20 minutes before or simultaneously with first antibiotic dose 1-2 mgkg ivim once maintenance 1-1. Your list will be saved and can be edited at any time. .

All material on this website is protected by copyright, copyright 1994-2018 by webmd llc. Please confirm that you would like to log out of medscape. Poivim divided q6hr, starting 24 hours before extubation and continued for 4-6 doses afterward 6 weeks 0.

By clicking send, you acknowledge that you have permission to email the recipient with this information. Decreases inflammation by suppressing migration of polymorphonuclear leukocytes (pmns) and reducing capillary permeability stabilizes cell and lysosomal membranes, increases surfactant synthesis, increases serum vitamin a concentration, and inhibits prostaglandin and proinflammatory cytokines suppresses lymphocyte proliferation through direct cytolysis, inhibits mitosis, breaks down granulocyte aggregates, and improves pulmonary microcirculation onset between a few minutes and several hours dependent on indication and route of administration additive aminophylline, bleomycin, cimetidine, floxacillin, furosemide, granisetron, lidocaine, meropenem, mitomycin, nafcillin, netilmicin, ondansetron, prochlorperazine, ranitidine, verapamil syringe caffeine, granisetron, metoclopramide, ondansetron, ranitidine, sufentanil y-site (partial list) acyclovir, allopurinol, cisplatin, cladribine, cyclophosphamide, cytarabine, docetaxel, etoposide phosphate, famotidine, fentanyl, fluconazole, gemcitabine, heparin with hydrocortisone, linezolid, lorazepam, meperidine, morphine, potassium chloride, propofol, sodium bicarbonate, zidovudine additive amikacin(?), daunorubicin, diphenhydramine with lorazepam and metoclopramide, metaraminol, vancomycin y-site ciprofloxacin, fenoldopam, idarubicin, methotrexate(?), midazolam, topotecan dexamethasone sodium phosphate administered by iv push, continuous or intermittent iv infusion, or im adding plans allows you to compare formulary status to other drugs in the same class. The above information is provided for general informational and educational purposes only.

The recipient will receive more details and instructions to access this offer. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk. Drugs that have restrictions other than prior authorization, quantity limits, and step therapy associated with each prescription.

Iv, then 4 mg im q6hr until clinical improvement is observed may be reduced after 2-4 days and gradually discontinued over 5-7 days for control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, and serum sickness overnight test 1 mg po between 1100 pm and midnight cortisol level tested between 800 and 900 am on following morning standard 2-day test 0. This restriction typically limits the quantity of the drug that will be covered. Medscape prescription drug monographs are based on fda-approved labeling information, unless otherwise noted, combined with additional data derived from primary medical literature. This restriction typically requires that certain criteria be met prior to approval for the prescription. Po q6hr (900 am, 300 pm, 900 pm, 300 am) for 2 days cortisol level tested 6 hours after final dose (900 am) confirmed cushing syndrome in which further workup is needed to identify whether hormone excess is the result of cushing syndrome or other causes standard 2-day test after determination of baseline serum cortisol or 24-hr urinary free cortisol, 2 mg po q6hr for 2 days urine for free cortisol is collected during test, and serum cortisol is checked 6 hours after final dose overnight test after determination of baseline serum cortisol, 8 mg (typically) po between 1100 pm and midnight cortisol level tested between 800 and 900 am on following morning iv test after determination of baseline serum cortisol, 1 mghr by continuous iv infusion for 5-7 hours 8-12 mg poiv alone or in combination with other antiemetics before chemotherapy, then 8 mg poiv q24hr for 1-3 days after chemotherapy (days 2-4) 2 mg po q6hr or 4 mg po q12hr beginning on day of ascent may be discontinued after 2- to 3-day stay at same elevation or initiation of descent high-altitude cerebral edema (hace) 8 mg once followed by 4 mg poivim q6hr until symptoms resolve 0.


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Drugs & Diseases. dexamethasone (Rx). Brand and Other Names:Decadron, Dexamethasone Intensol, more. ... Acute mountain sickness (AMS): 4 mg PO/IV/ IM q6hr; High-altitude cerebral edema (HACE): 8 mg once followed by 4 mg PO/ IV/IM ..... Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland ...
Buy Decadron 8mg 120 pills in Indianapolis Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland . Please confirm that you would like to log out of medscape. (Prescribers. 30-day-supply drugs cost $5 ( tier 1), $10 (tier 2) or $15 (tier 3). OTC: Over the counter medication available with a prescription. Can you hear me OK? cinemu. DEXAMETHASONE 0. Your list will be saved and can be edited at any time. Brand and Other Names:Decadron, Dexamethasone Intensol, Poivim divided q6hr, starting 24 hours before extubation and continued for 4-6 doses afterward 6 weeks 0. Decadron dexamethasone oral solution dexamethasone oral tablet. dexamethasone (Rx). Medscape prescription drug monographs are based on fda-approved labeling information, unless otherwise noted, combined with additional data derived from primary medical literature. This restriction requires that specific clinical criteria be met prior to the approval of the prescription.
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    All material on this website is protected by copyright, copyright 1994-2018 by webmd llc. Drugs that have restrictions other than prior authorization, quantity limits, and step therapy associated with each prescription. This restriction requires that specific clinical criteria be met prior to the approval of the prescription. Poivim divided q6hr, starting 24 hours before extubation and continued for 4-6 doses afterward 6 weeks 0. Iv divided q6hr for first 2-4 days of antibiotic therapy, starting 10-20 minutes before or simultaneously with first antibiotic dose 1-2 mgkg ivim once maintenance 1-1.

    Controlled studies in pregnant women show no evidence of fetal risk. Medscape prescription drug monographs are based on fda-approved labeling information, unless otherwise noted, combined with additional data derived from primary medical literature. This restriction typically limits the quantity of the drug that will be covered. Your list will be saved and can be edited at any time. Psychic derangements may appear when corticosteroids are used, ranging from euphoria, insomnia, mood swings, personality changes, and severe depression, to frank psychotic manifestations existing emotional instability or psychotic tendencies may also be aggravated by corticosteroids may have systemic and local effects examine joint fluid, as necessary to exclude a septic process avoid injection into infected site frequent intra-articular injections may result in damage to joint tissue if exposed to chickenpox, prophylaxis with varicella zoster immune globulin (vzig) may be indicated if exposed to measles, prophylaxis with immune globulin (ig) may be indicated if chickenpox develops, treatment with antiviral agents should be considered 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 prolonged corticosteroid use may result in elevated intraocular pressure, glaucoma, or cataracts with possible damage to optic nerves, and may enhance establishment of secondary ocular infections due to bacteria, fungi, or viruses consider referral to ophthalmologist for patients who develop ocular symptoms or use corticosteroid-containing products for more than 6 weeks 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 addisons disease) serious neurologic events, some resulting in death, have been reported with epidural injection specific events reported include, but are not limited to, spinal cord infarction, paraplegia, quadriplegia, cortical blindness, and stroke these serious neurologic events have been reported with and without use of fluoroscopy safety and effectiveness of epidural administration of corticosteroids have not been established, and corticosteroids are not approved for this use generally acceptable.

    The above information is provided for general informational and educational purposes only. Ivim divided q4-6hr not to exceed 16 mgday plasma cortisol level then determined at 800 am on following morning level will be decreased in normal individuals but at baseline level in cushing syndrome cardiovascular bradycardia, cardiac arrest, cardiac arrhythmias, cardiac enlargement, circulatory collapse, congestive heart failure, fat embolism, hypertension, hypertrophic cardiomyopathy in premature infants, myocardial rupture following recent myocardial infarction, edema, pulmonary edema, syncope, tachycardia, thromboembolism, thrombophlebitis, vasculitis dermatologic acne, allergic dermatitis, dry scaly skin, ecchymoses and petechiae, erythema, impaired wound healing, increased sweating, rash, striae, suppression of reactions to skin tests, thin fragile skin, thinning scalp hair, urticaria endocrine decreased carbohydrate and glucose tolerance, development of cushingoid state, hyperglycemia, glycosuria, hirsutism, hypertrichosis, increased requirements for insulin or oral hypoglycemic agents in diabetes, manifestations of latent diabetes mellitus, menstrual irregularities, secondary adrenocortical and pituitary unresponsiveness (particularly in times of stress, as in trauma, surgery, or illness), suppression of growth in pediatric patients fluid and electrolyte disturbances congestive heart failure in susceptible patients, fluid retention, hypokalemic alkalosis, potassium loss, sodium retention, tumor lysis syndrome gastrointestinal abdominal distention, elevation in serum liver enzyme levels (usually reversible upon discontinuation), hepatomegaly, increased appetite, nausea, pancreatitis, peptic ulcer with possible perforation and hemorrhage, perforation of the small and large intestine (particularly in patients with inflammatory bowel disease), ulcerative esophagitis metabolic negative nitrogen balance due to protein catabolismmusculoskeletal aseptic necrosis of femoral and humeral heads, loss of muscle mass, muscle weakness, osteoporosis, pathologic fracture of long bones, steroid myopathy, tendon rupture, vertebral compression fractures neurologicalpsychiatric convulsions, depression, emotional instability, euphoria, headache, increased intracranial pressure with papilledema (pseudotumor cerebri) usually following discontinuation of treatment, insomnia, mood swings, neuritis, neuropathy, paresthesia, personality changes, psychic disorders, vertigo ophthalmic exophthalmos, glaucoma, increased intraocular pressure, posterior subcapsular cataracts, vision blurred other abnormal fat deposits, decreased resistance to infection, hiccups, increased or decreased motility and number of spermatozoa, malaise, moon face, weight gain administration of live or live, attenuated vaccines is contraindicated in patients receiving immunosuppressive doses of corticosteroids use with caution in cirrhosis, diverticulitis, myasthenia gravis, peptic ulcer disease, ulcerative colitis, renal insufficiency, pregnancy average and large doses of corticosteroids can cause elevation of blood pressure, sodium and water retention, and increased excretion of potassium these effects are less likely to occur with synthetic derivatives except when used in large doses dietary salt restriction and potassium supplementation may be necessary all corticosteroids increase calcium excretion literature reports suggest apparent association between use of corticosteroids and left ventricular free wall rupture after recent myocardial infarction therapy with corticosteroids should be used with great caution in these patients corticosteroids can produce reversible hypothalamic-pituitary adrenal (hpa) axis suppression with potential for glucocorticosteroid insufficiency after withdrawal of treatment adrenocortical insufficiency may result from too rapid withdrawal may be minimized by gradual reduction of dosage relative insufficiency may persist for months after discontinuation of therapy therefore, in any situation of stress occurring during that period, reinstitute hormone therapy if patient is receiving steroids already, may increase dosage metabolic clearance of corticosteroids is decreased in hypothyroid patients and increased in hyperthyroid patients changes in thyroid status of patient may necessitate adjustment in dosage corticosteroids may exacerbate systemic fungal infections not for use in presence of such infections unless needed to control life-threatening drug reactions concomitant use of amphotericin b and hydrocortisone followed by cardiac enlargement and congestive heart failure reported latent disease may be activated or there may be an exacerbation of intercurrent infections due to pathogens, including those caused by amoeba, candida, cryptococcus, mycobacterium, nocardia, pneumocystis, toxoplasma rule out latent amebiasis or active amebiasis before initiating corticosteroid therapy in any patient who has spent time in the tropics or any patient with unexplained diarrhea corticosteroids should be used with great care in patients with known or suspected strongyloides (threadworm) infestation corticosteroid-induced immunosuppression may lead to strongyloides hyperinfection and dissemination with widespread larval migration, often accompanied by severe enterocolitis and potentially fatal gram-negative septicemia not for use in cerebral malaria close observation necessary if corticosteroids are indicated in patients with latent tuberculosis or tuberculin reactivity reactivation of the disease may occur during prolonged corticosteroid therapy, these patients should receive chemoprophylaxis use of oral corticosteroids not recommended in treatment of optic neuritis and may lead to increase in risk of new episodes corticosteroids should not be used in active ocular herpes simplex use lowest possible dose to control condition under treatment riskbenefit 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 may lead to inhibition of bone growth in pediatric patients and development of osteoporosis at any age special consideration should be given to patients at increased risk of osteoporosis (e. By clicking send, you acknowledge that you have permission to email the recipient with this information. Animal studies show risk and human studies not available or neither animal nor human studies done. Po q6hr (900 am, 300 pm, 900 pm, 300 am) for 2 days cortisol level tested 6 hours after final dose (900 am) confirmed cushing syndrome in which further workup is needed to identify whether hormone excess is the result of cushing syndrome or other causes standard 2-day test after determination of baseline serum cortisol or 24-hr urinary free cortisol, 2 mg po q6hr for 2 days urine for free cortisol is collected during test, and serum cortisol is checked 6 hours after final dose overnight test after determination of baseline serum cortisol, 8 mg (typically) po between 1100 pm and midnight cortisol level tested between 800 and 900 am on following morning iv test after determination of baseline serum cortisol, 1 mghr by continuous iv infusion for 5-7 hours 8-12 mg poiv alone or in combination with other antiemetics before chemotherapy, then 8 mg poiv q24hr for 1-3 days after chemotherapy (days 2-4) 2 mg po q6hr or 4 mg po q12hr beginning on day of ascent may be discontinued after 2- to 3-day stay at same elevation or initiation of descent high-altitude cerebral edema (hace) 8 mg once followed by 4 mg poivim q6hr until symptoms resolve 0. Decreases inflammation by suppressing migration of polymorphonuclear leukocytes (pmns) and reducing capillary permeability stabilizes cell and lysosomal membranes, increases surfactant synthesis, increases serum vitamin a concentration, and inhibits prostaglandin and proinflammatory cytokines suppresses lymphocyte proliferation through direct cytolysis, inhibits mitosis, breaks down granulocyte aggregates, and improves pulmonary microcirculation onset between a few minutes and several hours dependent on indication and route of administration additive aminophylline, bleomycin, cimetidine, floxacillin, furosemide, granisetron, lidocaine, meropenem, mitomycin, nafcillin, netilmicin, ondansetron, prochlorperazine, ranitidine, verapamil syringe caffeine, granisetron, metoclopramide, ondansetron, ranitidine, sufentanil y-site (partial list) acyclovir, allopurinol, cisplatin, cladribine, cyclophosphamide, cytarabine, docetaxel, etoposide phosphate, famotidine, fentanyl, fluconazole, gemcitabine, heparin with hydrocortisone, linezolid, lorazepam, meperidine, morphine, potassium chloride, propofol, sodium bicarbonate, zidovudine additive amikacin(?), daunorubicin, diphenhydramine with lorazepam and metoclopramide, metaraminol, vancomycin y-site ciprofloxacin, fenoldopam, idarubicin, methotrexate(?), midazolam, topotecan dexamethasone sodium phosphate administered by iv push, continuous or intermittent iv infusion, or im adding plans allows you to compare formulary status to other drugs in the same class. . Iv, then 4 mg im q6hr until clinical improvement is observed may be reduced after 2-4 days and gradually discontinued over 5-7 days for control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, and serum sickness overnight test 1 mg po between 1100 pm and midnight cortisol level tested between 800 and 900 am on following morning standard 2-day test 0. This restriction typically requires that certain criteria be met prior to approval for the prescription. Please confirm that you would like to log out of medscape.

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    This restriction requires that specific clinical criteria be met prior to the approval of the prescription. Please confirm that you would like to log out of medscape. Iv, then 4 mg im q6hr until clinical improvement is observed may be reduced after 2-4 days and gradually discontinued over 5-7 days for control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, and serum sickness overnight test 1 mg po between 1100 pm and midnight cortisol level tested between 800 and 900 am on following morning standard 2-day test 0...

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    Po q6hr (900 am, 300 pm, 900 pm, 300 am) for 2 days cortisol level tested 6 hours after final dose (900 am) confirmed cushing syndrome in which further workup is needed to identify whether hormone excess is the result of cushing syndrome or other causes standard 2-day test after determination of baseline serum cortisol or 24-hr urinary free cortisol, 2 mg po q6hr for 2 days urine for free cortisol is collected during test, and serum cortisol is checked 6 hours after final dose overnight test after determination of baseline serum cortisol, 8 mg (typically) po between 1100 pm and midnight cortisol level tested between 800 and 900 am on following morning iv test after determination of baseline serum cortisol, 1 mghr by continuous iv infusion for 5-7 hours 8-12 mg poiv alone or in combination with other antiemetics before chemotherapy, then 8 mg poiv q24hr for 1-3 days after chemotherapy (days 2-4) 2 mg po q6hr or 4 mg po q12hr beginning on day of ascent may be discontinued after 2- to 3-day stay at same elevation or initiation of descent high-altitude cerebral edema (hace) 8 mg once followed by 4 mg poivim q6hr until symptoms resolve 0...

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    Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk. Drugs that have restrictions other than prior authorization, quantity limits, and step therapy associated with each prescription. Your list will be saved and can be edited at any time. . Controlled studies in pregnant women show no evidence of fetal risk.

    Poivim divided q6hr, starting 24 hours before extubation and continued for 4-6 doses afterward 6 weeks 0. Iv, then 4 mg im q6hr until clinical improvement is observed may be reduced after 2-4 days and gradually discontinued over 5-7 days for control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, and serum sickness overnight test 1 mg po between 1100 pm and midnight cortisol level tested between 800 and 900 am on following morning standard 2-day test 0...