topimax filmuhúðuð tafla 200 mg
janssen-cilag ab - topiramatum inn - filmuhúðuð tafla - 200 mg
topimax filmuhúðuð tafla 25 mg
janssen-cilag ab - topiramatum inn - filmuhúðuð tafla - 25 mg
topimax filmuhúðuð tafla 50 mg
janssen-cilag ab - topiramatum inn - filmuhúðuð tafla - 50 mg
topimax hart hylki 15 mg
janssen-cilag ab - topiramatum inn - hart hylki - 15 mg
topiramat actavis filmuhúðuð tafla 100 mg
actavis group ptc ehf. - topiramatum inn - filmuhúðuð tafla - 100 mg
topiramat actavis filmuhúðuð tafla 25 mg
actavis group ptc ehf. - topiramatum inn - filmuhúðuð tafla - 25 mg
topiramat actavis filmuhúðuð tafla 50 mg
actavis group ptc ehf. - topiramatum inn - filmuhúðuð tafla - 50 mg
topiramate alvogen (topiramate portfarma) filmuhúðuð tafla 25 mg
alvogen ehf. - topiramatum inn - filmuhúðuð tafla - 25 mg
topiramate alvogen (topiramate portfarma) filmuhúðuð tafla 50 mg
alvogen ehf. - topiramatum inn - filmuhúðuð tafla - 50 mg
pylclari
curium pet france - piflufolastat (18f) - blöðruhálskirtli - greining geislavirkja - Þetta lyf er eingöngu ætlað til greiningar. pylclari is indicated for the detection of prostate-specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high-risk pca prior to initial curative therapy,to localize recurrence of pca in patients with a suspected recurrence based on increasing serum prostate-specific antigen (psa) levels after primary treatment with curative intent. pylclari is indicated for use with positron emission tomography (pet).