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Kripton (Bromocriptine)
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Bromocriptine

Effect of Kripton (CB-154) on oestrogen-induced prolactin release. The activity of 2-bromo-alpha-ergokryptine (Kripton) (5 mg kg-1, i.p.) on adenylate cyclase and on phosphodiesterase (PDE-PDE II) of rat striatum, has been examined both in vitro and in vivo.

Other names for this medication:
Bromocriptine, Parlodel, Brameston, Bromed, Bromergon, Bromocriptina, Bromodel, Cripsa, Criten, Cycloset, Deparo, Ergoset, Gynodel, Kirim, Kripton, Kriptonal, Melen, Pravidel,

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Kripton belongs to the group of medicines known as ergot alkaloids. Kripton blocks the release of a hormone called prolactin from the pituitary gland. Prolactin affects the menstrual cycle and milk production.

Kripton is used to treat certain menstrual problems (eg, amenorrhea) in women and stops milk production in some men and women who have abnormal milk leakage. It is also used to treat infertility in both men and women that occurs because the body is making too much prolactin.

Kripton is also used to treat acromegaly (overproduction of growth hormone) and pituitary prolactinomas (tumors of the pituitary gland).

Kripton is also used to treat the signs and symptoms of Parkinson's disease, often in combination with levodopa.

Kripton is also used together with proper diet and exercise to lower blood sugar levels in patients with type 2 diabetes.

This medicine is available only with your doctor's prescription.

This product is available in the following dosage forms:

  • Tablet
  • Capsule

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Parenteral and rectal use of 3-(1-phenylpropyl)-4-oxy-coumarin (marcunar) at the start of thrombosis prophylaxis As learned resourcefulness was negatively correlated with chemotherapy-related fatigue in patients with NHL, having this personality trait may help those patients manage fatigue. Comparative histochemical distribution of nerve fibres storing noradrenaline and neuropeptide Y (NPY) in human ovary, fallopian tube, and uterus. The elective treatment for metastatic disease is represented, in the vast majority of cases, by systemic chemotherapy with different schedules according to pathological diagnosis. In 56 non-obese and obese juveniles, a significantly positive correlation was found between age (6-18 years) and 24 h urine insulin and c-peptide, thus indicating that the age-related absolute value of body weight significantly affects insulin and c-peptide excretions both in non-obese and obese subjects.

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