Unione Europea - maltese - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - pneumococcal polysaccharide conjugate vaccine (adsorbed) - infezzjonijiet pnewmokokkali - pneumococcus, purified polysaccharides antigen conjugated - vaxneuvance is indicated for active immunisation for the prevention of invasive disease, pneumonia and acute otitis media caused by streptococcus pneumoniae in infants, children and adolescents from 6 weeks to less than 18 years of age. vaxneuvance is indicated for active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. ara t-taqsimiet 4. 4 u 5. 1 għal informazzjoni dwar il-protezzjoni kontra serotipi pnewmokokkiċi speċifiċi. the use of vaxneuvance should be in accordance with official recommendations.

Unione Europea - maltese - EMA (European Medicines Agency)

eli lilly nederland b.v. - duloxetine - neuropatiji dijabetiċi - psychoanaleptics, - trattament ta 'uġigħ newropatiku periferali dijabetiku. ariclaim huwa indikat fl-adulti.

Unione Europea - maltese - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - duloxetine - neuropatiji dijabetiċi - psychoanaleptics, - trattament ta 'uġigħ newropatiku periferali dijabetiku fl-adulti.

Unione Europea - maltese - EMA (European Medicines Agency)

zentiva, k.s. - duloxetine - neuralgia; depressive disorder, major; anxiety disorders; diabetes mellitus - anti-depressanti oħrajn - disturb depressiv tal-kura, uġigħ newropatiku dijabetiku, disturb ta 'ansjetà. duloxetine zentiva hu indikat fl-adulti.

Unione Europea - maltese - EMA (European Medicines Agency)

jenson pharmaceutical services limited - dextromethorphan, quinidine - manifestazzjonijiet ta 'mard newboliku - drogi oħra tas-sistema nervuża - nuedexta huwa indikat għat-trattament sintomatiku ta 'l-effett ta' pseudobulbar (pba) fl-adulti. l-effikaċja ġiet studjata biss f'pazjenti bi sklerożi laterali amjotrofika sottostanti jew sklerosi multipla.

Unione Europea - maltese - EMA (European Medicines Agency)

dechra regulatory b.v. - mirtazapine - psychoanaleptics, antidepressants in combination with psycholeptics - qtates - għall-piż tal-ġisem jiksbu fil-qtates jesperjenzaw foqra fl-aptit u l-piż tal-telf li jirriżulta minn mard kroniku tal-kundizzjonijiet mediċi.

Unione Europea - maltese - EMA (European Medicines Agency)

ucb pharma s.a.   - fenfluramine hydrochloride - epilepsies, myoclonic - anti-epilettiċi, - treatment of seizures associated with dravet syndrome as an add-on therapy to other antiepileptic medicines for patients 2 years of age and older. fintepla is indicated for the treatment of seizures associated with dravet syndrome and lennox-gastaut syndrome as an add-on therapy to other anti-epileptic medicines for patients 2 years of age and older.

Unione Europea - maltese - EMA (European Medicines Agency)

eli lilly nederland b.v. - lasmiditan succinate - disturbi fl-emigranja - analġeżiċi - rayvow is indicated for the acute treatment of the headache phase of migraine attacks, with or without aura in adults.

Unione Europea - maltese - EMA (European Medicines Agency)

otsuka pharmaceutical netherlands b.v. - aripiprazole - schizophrenia; bipolar disorder - psikolettiċi - abilify huwa indikat għat-trattament tal-iskiżofrenja fl-adulti u fl-adolexxenti ta '15-il sena jew ikbar. abilify huwa indikat għat-trattament ta 'episodji manijaċi serji f'disturb bipolari i u għall-prevenzjoni ta' episodju manijaku ġdid f'adulti li esperjenzaw episodji predominantament manijaċi u li l-episodji manijaċi rrispondew għat-trattament b'aripiprazole. abilify huwa indikat għat-trattament sa 12-il ġimgħa ta 'episodji manijaċi serji f'disturb bipolari i fl-adolexxenti ta' minn 13-il sena u anzjani.

Unione Europea - maltese - EMA (European Medicines Agency)

otsuka pharmaceutical netherlands b.v. - aripiprazole - skizofrenija - psikolettiċi - trattament ta 'manteniment ta' l-iskiżofrenja f'pazjenti adulti stabbli ma 'aripiprazole orali.