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Cinie (Sumatriptan)

Cinie succinate, a specific 5-HT1 receptor agonist, does not necessitate adjunctive antiemetics. Using clinical data from repeated migraine attacks treated with placebo, naratriptan 2.5 mg or Cinie 100 mg, we show that attack and interictal periods can be described by a random probability distribution.

Other names for this medication:
Sumatriptan, Imitrex, Amigrenex, Amigrenin, Cinie, Forcet, Formigran, Imigran, Imigrane, Imiject, Migranol, Migrastat, Migrex, Nograine, Sitran, Suma, Sumagen, Sumamigren, Sumatab, Sumatran, Sumetrin, Sumigran, Suminat, Sumitran, Sumitrex, Suvalan, Zumo,

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Cinie is used to treat acute migraine headaches in adults. It is not used to prevent migraine headaches and is not used for cluster headaches. Cinie works in the brain to relieve the pain from migraine headaches. It belongs to the group of medicines called triptans.

Many people find that their headaches go away completely after they take Cinie. Other people find that their headaches are much less painful, and that they are able to go back to their normal activities even though their headaches are not completely gone. Cinie often relieves other symptoms that occur together with a migraine headache, such as nausea, vomiting, sensitivity to light, and sensitivity to sound.

Cinie is not an ordinary pain reliever. It will not relieve pain other than from migraine headaches. This medicine is usually used for people whose headaches are not relieved by acetaminophen, aspirin, or other pain relievers.

Cinie has caused serious side effects in some people, especially people who have heart or blood vessel disease. Be sure that you discuss with your doctor the risks of using this medicine as well as the benefits that it can have.

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

This product is available in the following dosage forms:

  • Tablet

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an increase in the intra-macrophage redox state by GSH-C4 and I-152 enhances Th1 cytokine production although the chemical structure and the intra-cellular metabolism influence differently signalling pathways involved in IL-27 or IL-12 production. To investigate whether amylin might modulate digestive enzyme secretion from the exocrine pancreas, anesthetized Sprague Dawley rats were cannulated via the pancreatic duct and the secretory response (flow, amylase and lipase) to cholecystokinin (1 microg s.c.) was measured in the absence and in the presence of 0.1, 0.3 and 1 microg s.c. These results suggest that helichrysetin has great potentials for development as an anticancer agent.

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