spravato 28 mg/200mcl
مستودع أدوية أداتكو - adatco drug store - esketamine hcl 28 mg/200mcl - 28 mg/200mcl
spravato 28 mg nasal solution (spray)
janssen pharmaceuticals, inc.; importer: johnson & johnson (philippines), inc. - esketamine (as hydrochloride) - nasal solution (spray) - 28 mg
spravato 28 mg burun spreyİ, çözeltİ, 1 adet
johnson and johnson sihhİ mal. san. ve tİc. ltd. Ştİ. - esketamin hidroklorür -
spravato 28 mg burun spreyİ, çözeltİ, 2 adet
johnson and johnson sihhİ mal. san. ve tİc. ltd. Ştİ. - esketamin hidroklorür -
spravato solución para pulverización nasal 28 mg (esketamina)
johnson & johnson de chile s.a. - esketamina - esketamina clorhidrato 37,100 mg - spravato está indicado, en combinación con un antidepresivo oral, para el tratamiento de depresión resistente al tratamiento (drt) en adultos
syndros- dronabinol solution
insys therapeutics, inc. - dronabinol (unii: 7j8897w37s) (dronabinol - unii:7j8897w37s) - dronabinol 5 mg in 1 ml - syndros is indicated in adults for the treatment of: - anorexia associated with weight loss in patients with acquired immune deficiency syndrome (aids). - nausea and vomiting associated with cancer chemotherapy in patients who have failed to respond adequately to conventional antiemetic treatments. syndros is contraindicated in patients: - with a history of a hypersensitivity reaction to dronabinol. reported hypersensitivity reactions to dronabinol include lip swelling, hives, disseminated rash, oral lesions, skin burning, flushing, throat tightness [see adverse reactions (6.2)] . - with a history of a hypersensitivity reaction to alcohol. - who are receiving, or have recently received, disulfiram- or metronidazole-containing products within 14 days [see warning and precautions (5.3)] . syndros contains 50% (w/w) dehydrated alcohol and 5.5% (w/w) propylene glycol. risk summary syndros, a synthetic cannabinoid containing alcohol, may cause fetal harm. avoid use of syndros in pregnant women. although there is l
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