Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

deutsche homöopathie-union dhu-arzneimittel gmbh & co. kg. (3115488) - plantago major (pot.-angaben) - urtinktur - plantago major (pot.-angaben) (06414) 1 milliliter

Vereinigte Staaten - Englisch - NLM (National Library of Medicine)

yaopharma co., ltd. - venlafaxine hydrochloride (unii: 7d7rx5a8mo) (venlafaxine - unii:grz5rcb1qg) - venlafaxine 25 mg - venlafaxine tablets, usp are indicated for the treatment of major depressive disorder. the efficacy of venlafaxine tablets, usp in the treatment of major depressive disorder was established in 6-week controlled trials of adult outpatients whose diagnoses corresponded most closely to the dsm-iii or dsm-iii-r category of major depression and in a 4-week controlled trial of inpatients meeting diagnostic criteria for major depression with melancholia (see clinical trials). a major depressive episode implies a prominent and relatively persistent depressed or dysphoric mood that usually interferes with daily functioning (nearly every day for at least 2 weeks); it should include at least four of the following eight symptoms: change in appetite, change in sleep, psychomotor agitation or retardation, loss of interest in usual activities or decrease in sexual drive, increased fatigue, feelings of guilt or worthlessness, slowed thinking or impaired concentration, and a suicide attempt or suicidal ideation. the efficacy of venlafaxine hydrochloride extended-release capsules in maintaining an antidepressant response for up to 26 weeks following 8 weeks of acute treatment was demonstrated in a placebo-controlled trial. the efficacy of venlafaxine tablets, usp in maintaining an antidepressant response in patients with recurrent depression who had responded and continued to be improved during an initial 26 weeks of treatment and were then followed for a period of up to 52 weeks was demonstrated in a second placebo-controlled trial (see clinical trials). nevertheless, the physician who elects to use venlafaxine tablets/venlafaxine hydrochloride extended-release capsules for extended periods should periodically reevaluate the long-term usefulness of the drug for the individual patient. hypersensitivity to venlafaxine hydrochloride or to any excipients in the formulation. the use of maois intended to treat psychiatric disorders with venlafaxine or within 7 days of stopping treatment with venlafaxine is contraindicated because of an increased risk of serotonin syndrome. the use of venlafaxine within 14 days of stopping an maoi intended to treat psychiatric disorders is also contraindicated (see warnings and dosage and administration). starting venlafaxine 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). venlafaxine tablets are not a controlled substance. in vitro studies revealed that venlafaxine has virtually no affinity for opiate, benzodiazepine, phencyclidine (pcp), or n-methyl-d-aspartic acid (nmda) receptors. venlafaxine was not found to have any significant cns stimulant activity in rodents. in primate drug discrimination studies, venlafaxine showed no significant stimulant or depressant abuse liability. discontinuation effects have been reported in patients receiving venlafaxine (see dosage and administration). while venlafaxine has not been systematically studied in clinical trials for its potential for abuse, there was no indication of drug seeking behavior in the clinical trials. however, it is not possible to predict on the basis of premarketing experience the extent to which a cns active drug will be misused, diverted, and/or abused once marketed. consequently, physicians should carefully evaluate patients for history of drug abuse and follow such patients closely, observing them for signs of misuse or abuse of venlafaxine (e.g., development of tolerance, incrementation of dose, drug seeking behavior).

Europäische Union - Litauisch - EMA (European Medicines Agency)

eli lilly nederland b.v. - insulinas lispro - cukrinis diabetas - narkotikai, vartojami diabetu - suaugusiems ir vaikams, sergantiems cukriniu diabetu, kurie reikalauja insulino palaikyti normalią gliukozės homeostazę, gydyti. humalog taip pat skiriamas pradiniam cukrinio diabeto stabilizavimui.

Europäische Union - Italienisch - EMA (European Medicines Agency)

eli lilly nederland b.v. - insulina lispro - diabete mellito - farmaci usati nel diabete - per il trattamento di adulti e bambini con diabete mellito che necessitano di insulina per il mantenimento dell'omeostasi glicemica normale. humalog è anche indicato per la stabilizzazione iniziale del diabete mellito.

Türkei - Türkisch - TİTCK (Türkİye İlaç Ve Tibbİ Cİhaz Kurumu)

lİlly İlaÇ tİc. ltd. Ştİ. - % 25 insülin lispro, % 75 insülin lispro protamin - kombinasyonları

Türkei - Türkisch - TİTCK (Türkİye İlaç Ve Tibbİ Cİhaz Kurumu)

lİlly İlaÇ tİc. ltd. Ştİ. - % 25 insülin lispro, % 75 insülin lispro protamin - kombinasyonları

Türkei - Türkisch - TİTCK (Türkİye İlaç Ve Tibbİ Cİhaz Kurumu)

lİlly İlaÇ tİc. ltd. Ştİ. - % 50 insülin lispro, % 50 insülin lispro protamin - kombinasyonları

Europäische Union - Griechisch - EMA (European Medicines Agency)

eli lilly nederland b.v. - ινσουλίνη lispro - Σακχαρώδης διαβήτης - Φάρμακα που χρησιμοποιούνται στον διαβήτη - Για τη θεραπεία ενηλίκων και παιδιών με σακχαρώδη διαβήτη που χρειάζονται ινσουλίνη για τη διατήρηση της φυσιολογικής ομοιόστασης της γλυκόζης. Το humalog ενδείκνυται επίσης για την αρχική σταθεροποίηση του σακχαρώδους διαβήτη.

Europäische Union - Rumänisch - EMA (European Medicines Agency)

eli lilly nederland b.v. - insulina lispro - diabetul zaharat - medicamente utilizate în diabet - pentru tratamentul adulților și copiilor cu diabet zaharat care necesită insulină pentru menținerea homeostaziei normale a glucozei. humalog este de asemenea indicat pentru stabilizarea inițială a diabetului zaharat.

Europäische Union - Spanisch - EMA (European Medicines Agency)

eli lilly nederland b.v. - insulina lispro - diabetes mellitus - drogas usadas en diabetes - para el tratamiento de adultos y niños con diabetes mellitus que requieren insulina para el mantenimiento de la homeostasis normal de glucosa. humalog también está indicado para la estabilización inicial de la diabetes mellitus.