KAMRAB Israel - English - Ministry of Health

kamrab

kamada ltd, israel - human-rabies immunoglobulin - solution for injection - human-rabies immunoglobulin 150 iu/ml - rabies immunoglobulin - rabies immunoglobulin - kamrab im is indicated for passive, transient post-exposure prevention of rabies infection when given immediately to individuals in cases of contact with rabid or possibly rabid animal.

TERIPARATIDE KAMADA Israel - English - Ministry of Health

teriparatide kamada

kamada ltd, israel - teriparatide - solution for injection - teriparatide 0.250 mg / 1 ml - teriparatide - treatment of postmenopausal women with osteoporosis at high risk for fractureteriparatide kamada is indicated for the treatment of postmenopausal women with osteoporosis at high risk for fracture, defined as a history of osteoporotic fracture, multiple risk factors for fracture, or patients who have failed or are intolerant to other available osteoporosis therapy. in postmenopausal women with osteoporosis, teriparatide kamada increases bmd reduces the risk of vertebral and nonvertebral fractures.increase of bone mass in men with primary or hypogonadal osteoporosis at high risk for fractureteriparatide kamada is indicated to increase bone mass in men with primary or hypogonadal osteoporosis at high risk for fracture, defined as a history of osteoporotic fracture, multiple risk factors for fracture, or patients who have failed or are intolerant to other available osteoporosis therapy.treatment of men and women with glucocorticoid-induced osteoporosis at high risk for fractureteriparatide kamada is indicated for the treatment of men and women with osteoporosis associated with sustained systemic glucocorticoid therapy (daily dosage equivalent to 5 mg or greater of prednisone) at high risk for fracture, defined as a history of osteoporotic fracture, multiple risk factors for fracture, or patients who have failed or are intolerant to other available osteoporosis therapy.

GLASSIA Israel - English - Ministry of Health

glassia

kamada ltd, israel - alpha-1-antitrypsin ( aat) - solution for infusion - alpha-1-antitrypsin ( aat) 1 g / 50 ml - alfa1 antitrypsin - alpha1-proteinase inhibitor (human), glassia® is indicated for chronic augmentation and maintenance therapy in individuals with congenital deficiency of alpha1-proteinase inhibitor (alpha1-pi), also known as alpha1-antitrypsin (aat) deficiency and clinical evidence of emphysema.

BRAMITOB Israel - English - Ministry of Health

bramitob

kamada ltd, israel - tobramycin - solution for inhalation - tobramycin 300 mg / 4 ml - tobramycin - tobramycin - management of chronic pulmonary infection due to pseudomonas aeruginosa in patients with cystic fibrosis aged 6 years and older.

KAM-RHO (D) I.V. Israel - English - Ministry of Health

kam-rho (d) i.v.

kamada ltd, israel - anti-d immunoglobulins - solution for injection - anti-d immunoglobulins 150 mcg / 1 ml - anti-d (rh) immunoglobulin - anti-d (rh) immunoglobulin - suppression of rh immunization in non-sensitized rho(d) negative women delivering an rh positive baby, or when the baby's rh type is unknown. suppression of rh immunization after spontaneous or induced abortions, threatened abortion associated with maternal bleeding amniocentesis, chorionic villus sampling ruptured tubal pregnancy, and significant abdominal trauma. kam-rho should be given within 72 hours of event. immune thrombocytopenic purpura (itp): rho (d)-positive adults with chronic itp, children with chronic or acute itp, and patients with thrombocytopenia secondary to hiv infection in clinical situations requiring an increase in platelet count to prevent excessive hemorrhage.

KAM-RHO D I.M. Israel - English - Ministry of Health

kam-rho d i.m.

kamada ltd, israel - anti-d immunoglobulins - solution for injection - anti-d immunoglobulins 150 mcg/ml - anti-d (rh) immunoglobulin - anti-d (rh) immunoglobulin - pregnancy/other obstetric conditions, suppression of rh immunization in non-sensitized rh0 (d) negative women delivering an rh0 positive baby or when the baby's rh type is unknown. suppression of rh immunization after spontaneous or induced abortions threatened abortion associated with maternal bleeding amniocentesis chorionic villus sampling ruptured tubal pregnancy and significant abdominal trauma. kam rh0 -d im should be given within 72 hours of the event. it may be given even after up to one month although efficacy may be somewhat reduced.transfusion: suppression of rh isoimmunization in rh0 (d) antigen-negative patients transfused with rh0 (d) antigen-positive rbcs of blood components containing rh0 (d) antigen-positive rbcs . initate treatment within 72 hours of exposure.

ELIGARD 22.5 MG Israel - English - Ministry of Health

eligard 22.5 mg

kamada ltd, israel - leuprorelin acetate - powder and solvent for solution for injection - leuprorelin acetate 22.5 mg - eligard is indicated for the treatment of hormone dependent advanced prostate cancer and for the treatment of high-risk localized and locally advanced hormone dependent prostate cancer in combination with radiotherapy.

ELIGARD 45 MG Israel - English - Ministry of Health

eligard 45 mg

kamada ltd, israel - leuprorelin acetate - powder and solvent for solution for injection - leuprorelin acetate 45 mg - eligard is indicated for the treatment of hormone dependent advanced prostate cancer and for the treatment of high-risk localized and locally advanced hormone dependent prostate cancer in combination with radiotherapy.

ELIGARD 7.5 MG Israel - English - Ministry of Health

eligard 7.5 mg

kamada ltd, israel - leuprorelin acetate - powder and solvent for solution for injection - leuprorelin acetate 7.5 mg - eligard is indicated for the treatment of hormone dependent advanced prostate cancer and for the treatment of high-risk localized and locally advanced hormone dependent prostate cancer in combination with radiotherapy.

BRAMITOB Israel - English - Ministry of Health

bramitob

kamada ltd, israel - tobramycin - solution for inhalation - tobramycin 300 mg / 4 ml - tobramycin - management of chronic pulmonary infection due to pseudomonas aeruginosa in patients with cystic fibrosis aged 6 years and older.