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 Cabazitaxel
Cabazitaxel (previously XRP-6258, trade name Jevtana) is a semi-synthetic derivative of a natural taxoid.[1] It was developed by Sanofi-Aventis and was approved by the U.S. FDA for the treatment of hormone-refractory prostate cancer on June 17, 2010. It is a microtubule inhibitor, and the fourth taxane to be approved as a cancer therapy.[2][unreliable source?] Cabazitaxel in combination with prednisone is a treatment option for hormone-refractory prostate cancer following docetaxel-based trea...
 Cabergoline
Cabergoline (brand names Caberlin, Dostinex and Cabaser), an ergot derivative, is a potent dopamine receptor agonist on D2 receptors. Rat studies show cabergoline has a direct inhibitory effect on pituitary lactotroph (prolactin) cells.[1] It is frequently used as a first-line agent in the management of prolactinomas due to its higher affinity for D2 receptor sites, less severe side effects, and more convenient dosing schedule than the older bromocriptine. Contents 1 Uses 2 Off-label 3...
 Cabometyx Cabozantinib (S)-Malate
Cabozantinib, marketed under the trade name Cabometyx among others, is a small molecule inhibitor of the tyrosine kinases c-Met and VEGFR2, and has been shown to reduce tumor growth, metastasis, and angiogenesis. It was discovered and developed by Exelixis Inc. Cabozantinib was granted orphan drug status by the U.S. Food and Drug Administration (FDA) in January 2011.[1] Cabozantinib is approved by the U.S. FDA for medullary thyroid cancer.[2] and advanced renal cell carcinoma in people who ha...
 Cabozantinib S Malate
Cabozantinib, marketed under the trade name Cabometyx among others, is a small molecule inhibitor of the tyrosine kinases c-Met and VEGFR2, and has been shown to reduce tumor growth, metastasis, and angiogenesis. It was discovered and developed by Exelixis Inc. Cabozantinib was granted orphan drug status by the U.S. Food and Drug Administration (FDA) in January 2011.[1] Cabozantinib is approved by the U.S. FDA for medullary thyroid cancer.[2] and advanced renal cell carcinoma in people who ha...
 Caduet Amlodipine + Atorvastatin
The drug combination atorvastatin/amlodipine (trade names Caduet in the US, Australia and Russia, and Envacar elsewhere) is a medication approved by the Food and Drug Administration (FDA) for the treatment of high cholesterol and high blood pressure. It is a fixed-dose combination drug containing the calcium channel blocker amlodipine and the statin atorvastatin being marketed by the pharmaceutical company Pfizer.[1] References ^ "CADUET (amlodipine besylate/atorvastatin calcium) Tablets"...
 Caelyx Doxorubicin Liposomal
Doxorubicin, sold under the trade names Adriamycin among others, is a medication used in cancer chemotherapy. It is commonly used in the treatment of a wide range of cancers, including hematological malignancies (blood cancers, like leukaemia and lymphoma), many types of carcinoma (solid tumours) and soft tissue sarcomas.[3] It is often used in combination chemotherapy as a component of various chemotherapy regimens. Common adverse effects of doxorubicin include hair loss (seen in most of tho...
 Cafatine PB Belladonna + Caffeine + Ergotamine + Phentobarbital
Atropa belladonna, commonly known as belladonna or deadly nightshade, is a perennial herbaceous plant (rhizomatous hemicryptophyte) in the Nightshade family (which includes tomatoes, potatoes, eggplant, etc.) Solanaceae, native to Europe, North Africa, and Western Asia. Its distribution extends from Great Britain in the west to western Ukraine and the Iranian province of Gilan in the east. It is also naturalised and/or introduced in some parts of Canada and the United States. The foliage and ...
 Cafcit Caffeine
Caffeine is a central nervous system (CNS) stimulant of the methylxanthine class.[10] It is the world's most widely consumed psychoactive drug. Unlike many other psychoactive substances, it is legal and unregulated in nearly all parts of the world. There are several known mechanisms of action to explain the effects of caffeine. The most prominent is that it reversibly blocks the action of adenosine on its receptor and consequently prevents the onset of drowsiness induced by adenosine. Caffein...
 Cafergot Caffeine + Ergotamine
Caffeine/ergotamine (trade name Cafergot) is the proprietary name of a medication consisting of ergotamine tartrate and caffeine.[1] This combination is used for the treatment of vascular headaches, such as migraine headache. Contents 1 Use 2 Mechanism of action 3 Adverse effects 4 References Use Correct timing of use is important. Cafergot is an abortive headache treatment, which prevents the development of the headache, rather than a treatment for an established headache. The me...
 Caffeine
Caffeine is a central nervous system (CNS) stimulant of the methylxanthine class.[10] It is the world's most widely consumed psychoactive drug. Unlike many other psychoactive substances, it is legal and unregulated in nearly all parts of the world. There are several known mechanisms of action to explain the effects of caffeine. The most prominent is that it reversibly blocks the action of adenosine on its receptor and consequently prevents the onset of drowsiness induced by adenosine. Caffein...
 Caffeine + Ergotamine
Caffeine/ergotamine (trade name Cafergot) is the proprietary name of a medication consisting of ergotamine tartrate and caffeine.[1] This combination is used for the treatment of vascular headaches, such as migraine headache. Contents 1 Use 2 Mechanism of action 3 Adverse effects 4 References Use Correct timing of use is important. Cafergot is an abortive headache treatment, which prevents the development of the headache, rather than a treatment for an established headache. The me...
 Caffeine + Sodium Benzoate
Sodium benzoate is a substance which has the chemical formula NaC7H5O2. It is a widely used food preservative, with an E number of E211. It is the sodium salt of benzoic acid and exists in this form when dissolved in water. It can be produced by reacting sodium hydroxide with benzoic acid. Contents 1 Uses 1.1 Preservative 1.2 Pharmaceutical applications 1.3 Other uses 2 Mechanism of food preservation 3 Production 4 Health and safety 4.1 Association with benzene in soft drinks 4.2 H...
 Cal-Mag-Zinc
A multivitamin is a preparation intended to be a dietary supplement with vitamins, dietary minerals, and other nutritional elements. Such preparations are available in the form of tablets, capsules, pastilles, powders, liquids, and injectable formulations. Other than injectable formulations, which are only available and administered under medical supervision, multivitamins are recognized by the Codex Alimentarius Commission (the United Nations' authority on food standards) as a category of fo...
 Cal-Nate
Prenatal vitamins are vitamin and mineral supplements intended to be taken before and during pregnancy and during postnatal lactation. Although not intended to replace a healthy diet, prenatal vitamins provide women of child bearing age with nutrients recognized by the various health organizations including the American Dietetic Association as helpful for a healthy pregnancy outcome. It may be appropriate to start taking prenatal vitamins once the female enters childbearing age.[1] Prenatal v...
 Caladryl Calamine + Pramoxine
Pramocaine (INN and BAN, also known as pramoxine or pramoxine HCI) is a topical anesthetic discovered at Abbott Laboratories in 1953[1] and used as an antipruritic. During research and development, pramocaine hydrochloride stood out among a series of alkoxy aryl alkamine ethers as an especially good topical local anesthetic agent.[1] Pharmacologic study revealed it to be potent and of low acute and subacute toxicity, well tolerated by most mucous membranes and of a low sensitizing index in hu...
 Caladryl Clear Pramoxine + Zinc Acetate
Pramocaine (INN and BAN, also known as pramoxine or pramoxine HCI) is a topical anesthetic discovered at Abbott Laboratories in 1953[1] and used as an antipruritic. During research and development, pramocaine hydrochloride stood out among a series of alkoxy aryl alkamine ethers as an especially good topical local anesthetic agent.[1] Pharmacologic study revealed it to be potent and of low acute and subacute toxicity, well tolerated by most mucous membranes and of a low sensitizing index in hu...
 Calamine + Pramoxine
Pramocaine (INN and BAN, also known as pramoxine or pramoxine HCI) is a topical anesthetic discovered at Abbott Laboratories in 1953[1] and used as an antipruritic. During research and development, pramocaine hydrochloride stood out among a series of alkoxy aryl alkamine ethers as an especially good topical local anesthetic agent.[1] Pharmacologic study revealed it to be potent and of low acute and subacute toxicity, well tolerated by most mucous membranes and of a low sensitizing index in hu...
 Calan Verapamil
Verapamil (sold under various trade names)[1] is a calcium channel blocker used in the treatment of hypertension, angina pectoris, cardiac arrhythmia, and most recently, cluster headaches.[2][3] It is also an effective preventive medication for migraine.[4] Verapamil has also been used as a vasodilator during cryopreservation of blood vessels. Verapamil is of the phenylalkylamine class. It is a class-IV antiarrhythmic and more effective than digoxin in controlling ventricular rate.[5] It was ...
 Calan SR Verapamil
Verapamil (sold under various trade names)[1] is a calcium channel blocker used in the treatment of hypertension, angina pectoris, cardiac arrhythmia, and most recently, cluster headaches.[2][3] It is also an effective preventive medication for migraine.[4] Verapamil has also been used as a vasodilator during cryopreservation of blood vessels. Verapamil is of the phenylalkylamine class. It is a class-IV antiarrhythmic and more effective than digoxin in controlling ventricular rate.[5] It was ...
 Calcibind Cellulose Sodium Phosphate
Sodium cellulose phosphate is a drug used to treat hypercalcemia and hypercalciuria. It has been used to prevent kidney stones.[1][2] This compound is an ion-exchange resin that can not be absorbed by the body. However, it can be used to restore the normal intestinal calcium absorption. When it is taken orally, it binds strongly to calcium and inhibits its absorption into the blood. From there, inhibition is caused due to the lower intraluminal calcium levels, which is typically available for...

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