Zispin soltabs contain the active ingredient mirtazapine, which is a type of antidepressant. (NB. Mirtazapine is also available without a brand name, ie as the generic medicine.)

Mirtazapine works in the brain, where it enhances the effect of naturally occurring chemicals called neurotransmitters. These are chemical compounds that act as chemical messengers between nerve cells. Noradrenaline and serotonin are two such neurotransmitters and have various functions that we know of.

When noradrenaline and serotonin are released from nerve cells in the brain they act to lighten mood. When they are bound to nerve cells in the brain, they no longer have an effect on mood. It is thought that when depression occurs, there may be a decreased amount of noradrenaline and serotonin released from nerve cells in the brain.

Mirtazapine works by blocking receptors called alpha-2 receptors that are found on nerve cells in the brain. Noradrenaline and serotonin would normally bind to these receptors. By blocking them, mirtazapine prevents noradrenaline and serotonin from becoming bound to the nerve cells. This enhances the mood-lightening effect of free noradrenaline and serotonin that is released from nerve cells, and helps relieve depression.

Sovaldi is a hepatitis C virus (HCV) nucleotide analog NS5B polymerase inhibitor indicated for the treatment of chronic hepatitis C (CHC) infection as a component of a combination antiviral treatment regimen. Sovaldi (sofosbuvir) is an antiviral medication that prevents hepatitis C virus (HCV) cells from multiplying in your body.

Sovaldi is used in combination with other medications to treat hepatitis C in adults. Sovaldi is sometimes used in people who also have HIV, or people who have liver cancer and are going to have a liver transplant. This medicine is not a treatment for HIV or AIDS.

Sovaldi must be given in combination with other antiviral medications and should not be used alone. Sovaldi is usually given with ribavirin (Copegus, Rebetol, Ribasphere, RibaTab) with or without peginterferon alfa (Pegasys, PegIntron).

Sovaldi is used in combination with other medications, usually ribavirin with or without peginterferon alfa.

Read the medication guide or patient instructions provided with each medication in your combination therapy. Do not change your doses or medication schedule without your doctor's advice.

Slideshow 2013 Drug News Round-Up - Top 20 Stories 2013 Drug News Round-Up - Top 20 StoriesRibavirin can cause birth defects or death in an unborn baby. Do not use sofosbuvir with ribavirin if you are pregnant, or if you are a man and your female partner is pregnant.

Tamsulosin hydrochloride is an antagonist of alpha1A adrenoceptors in the prostate.

Tamsulosin hydrochloride is (-)-(R)-5-[2-[[2-(o-Ethoxyphenoxy) ethyl]amino]propyl]-2-methoxybenzenesulfonamide, monohydrochloride. Tamsulosin hydrochloride is a white crystalline powder that melts with decomposition at approximately 230C. It is sparingly soluble in water and methanol, slightly soluble in glacial acetic acid and ethanol, and practically insoluble in ether. The empirical formula of tamsulosin hydrochloride is C20H28N2O5S HCl. The molecular weight of tamsulosin hydrochloride is 444.98.

Each FLOMAX capsule for oral administration contains tamsulosin hydrochloride 0.4 mg, and the following inactive ingredients methacrylic acid copolymer dispersion, NF; microcrystalline cellulose, NF; triacetin, USP; calcium stearate, NF; talc, USP; FD&C blue No. 2; titanium dioxide; ferric oxide; gelatin, and trace amounts of black edible ink.

Analgin tablets are administered for the treatment of pains of various origin toothache, headache, arthralgia, neuralgia, myalgia, milder visceral pains, dysmenorrhea, as an antipyretic in the complex therapy of inflammatory diseases of upper respiratory tract, infectious diseases. Analgin solution for injection is used in cases of acute and severe pain after surgical operations or traumas; pains due to tumors; renal and biliary colics and high temperature unaffected by other drugs.

Hypersensitivity to metamizole and other pyrazolone derivatives; acute hepatic porphyria; inborn glucose-6-phosphate dehydrogenase deficiency; severe renal or hepatic diseases; hematologic diseases (aplastic anemia, leucopenia and agranulocytosis); first and last trimester of pregnancy. It should be avoided in lactating or pregnant women due to the lack of studies on its safety. Parenteral administration is contraindicated in children under 1 year.

Somatropin also commonly referred to as human growth hormone (HGH), is a hormone that is produced in the human body and excreted into the blood by the cells of the anterior pituitary gland. It is a single-chain protein that is composed of 191 amino acids with a molecular weight of approximately 22, 000 Daltons. It is used to treat growth failure in children and adults who lack natural growth hormone, and in those with chronic kidney failure, Noonan syndrome, Turner syndrome, short stature at birth with no catch-up growth, and other causes.Contact for detail.

Trazodone Hydrochloride used for the treatment of depression. However, it is sometimes prescribed as a sedative, and it also is used in combination with other drugs for the treatment of psychiatric conditions.

For the treatment of depression, the typical dose for adults is 150-600 mg per day. The initial dose usually is 150 mg per day. Trazodone is given in one or more divided doses, sometimes with the largest dose at night. Doses often are adjusted slowly upwards to find the optimal dose. Elderly patients and debilitated persons may need lower doses. Your physician will tell you your recommended dosage.

Selegiline hydrochloride is a levorotatory acetylenic derivative of phenethylamine. It is commonly referred to in the clinical and pharmacological literature as l- deprenyl.

The chemical name is (R)-(-)-N, -Dimethyl-N-2-propynylphenethylamine hydrochloride. It is a white to near white crystalline powder, freely soluble in water, chloroform, and methanol, and has a molecular weight of 223.75. The molecular formula is C13H17N.HCI. Each capsule, for oral administration contains 5 mg of Selegiline hydrochloride. In addition, each capsule contains the following inactive ingredients Anhydrous Lactose NF, Citric Acid Anhydrous USP, Microcrystalline Cellulose NF PH102, Stearic Acid NF and Talc USP. The capsule shell contains Gelatin NF, FD & C Blue #1 and Titanium Dioxide. The capsule logo ink Black SW-9008/SW-9009 contains the following inactive ingredients Ammonium Hydroxide; Black Iron Oxide, Bacteria Controlled EEC No. 172; n-Butyl NF; Ethyl Alcohol, Anhydrous, 200 Proof; Isopropyl Alcohol USP; Potassium Hydroxide NF; Propylene Glycol USP; Purified Water USP and Shellac NF.

An extremely poisonous white compound, KCN, used in the extraction of gold and silver from ores, in electroplating, and in photography, and as a fumigant and insecticide. (inorganic chemistry) The potassium salt of hydrocyanic acid, KCN; the colourless crystals are soluble in water, and it is extremely poisonous, and is used in electroplating, the extraction of gold and silver from their ores, and in photography.

vyvanse (lisdexamfetamine) is a central nervous system stimulant. It affects chemicals in the brain and nerves that contribute to hyperactivity and impulse control.

vyvanse is used to treat attention deficit hyperactivity disorder (adhd) in adults and in children who are at least 6 years old.

vyvanse may also be used for other purposes not listed in this medication guide.

do not use vyvanse if you have taken an mao inhibitor in the past 14 days. A dangerous drug interaction could occur. Mao inhibitors include isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, tranylcypromine, and others.

vyvanse is a drug of abuse and may be habit-forming. Keep track of the amount of medicine used from each new bottle. You should be aware if anyone is using your medicine improperly or without a prescription. Using this medication improperly can cause death or serious side effects on the heart.

you should not use vyvanse if you are allergic to lisdexamfetamine.

do not use vyvanse if you have taken an mao inhibitor in the past 14 days. A dangerous drug interaction could occur. Mao inhibitors include isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, tranylcypromine, and others.

some stimulants have caused sudden death in people with serious heart problems or congenital heart defects. Tell your doctor if you have heart disease, heart rhythm disorder;

coronary artery disease (hardened arteries); or history of heart attack.

to make sure this medicine is safe for you, tell your doctor if you have high blood pressure;

peripheral vascular disease such as raynaud's syndrome;

a personal or family history of mental illness, psychotic disorder, bipolar illness, depression, or suicide attempt; or

if you take an antidepressant.

Phenethylamine, or phenylethylamine is an organic compound and a natural monoamine alkaloid, a trace amine, and also the name of a class of chemicals with many members that are well known for their psychoactive and stimulant effects.

Phenylethylamine functions as a neuromodulator or neurotransmitter in the mammalian central nervous system. It is biosynthesized from the amino acid L-phenylalanine by enzymatic decarboxylation via the enzyme aromatic L-amino acid decarboxylase. In addition to its presence in mammals, phenethylamine is found in many other organisms and foods, such as chocolate, especially after microbial fermentation. It is sold as a dietary supplement for purported mood and weight loss-related therapeutic benefits; however, orally ingested phenethylamine experiences extensive first-pass metabolism by monoamine oxidase B (MAO-B), which turns it into phenylacetic acid. This prevents significant concentrations from reaching the brain when taken in low doses.

Zispin soltabs contain the active ingredient mirtazapine, which is a type of antidepressant. (NB. Mirtazapine is also available without a brand name, ie as the generic medicine.)

Mirtazapine works in the brain, where it enhances the effect of naturally occurring chemicals called neurotransmitters. These are chemical compounds that act as chemical messengers between nerve cells. Noradrenaline and serotonin are two such neurotransmitters and have various functions that we know of.

When noradrenaline and serotonin are released from nerve cells in the brain they act to lighten mood. When they are bound to nerve cells in the brain, they no longer have an effect on mood. It is thought that when depression occurs, there may be a decreased amount of noradrenaline and serotonin released from nerve cells in the brain.

Mirtazapine works by blocking receptors called alpha-2 receptors that are found on nerve cells in the brain. Noradrenaline and serotonin would normally bind to these receptors. By blocking them, mirtazapine prevents noradrenaline and serotonin from becoming bound to the nerve cells. This enhances the mood-lightening effect of free noradrenaline and serotonin that is released from nerve cells, and helps relieve depression.

Sovaldi is a hepatitis C virus (HCV) nucleotide analog NS5B polymerase inhibitor indicated for the treatment of chronic hepatitis C (CHC) infection as a component of a combination antiviral treatment regimen. Sovaldi (sofosbuvir) is an antiviral medication that prevents hepatitis C virus (HCV) cells from multiplying in your body.

Sovaldi is used in combination with other medications to treat hepatitis C in adults. Sovaldi is sometimes used in people who also have HIV, or people who have liver cancer and are going to have a liver transplant. This medicine is not a treatment for HIV or AIDS.

Sovaldi must be given in combination with other antiviral medications and should not be used alone. Sovaldi is usually given with ribavirin (Copegus, Rebetol, Ribasphere, RibaTab) with or without peginterferon alfa (Pegasys, PegIntron).

Sovaldi is used in combination with other medications, usually ribavirin with or without peginterferon alfa.

Read the medication guide or patient instructions provided with each medication in your combination therapy. Do not change your doses or medication schedule without your doctor's advice.

Slideshow 2013 Drug News Round-Up - Top 20 Stories 2013 Drug News Round-Up - Top 20 StoriesRibavirin can cause birth defects or death in an unborn baby. Do not use sofosbuvir with ribavirin if you are pregnant, or if you are a man and your female partner is pregnant.

Tamsulosin hydrochloride is an antagonist of alpha1A adrenoceptors in the prostate.

Tamsulosin hydrochloride is (-)-(R)-5-[2-[[2-(o-Ethoxyphenoxy) ethyl]amino]propyl]-2-methoxybenzenesulfonamide, monohydrochloride. Tamsulosin hydrochloride is a white crystalline powder that melts with decomposition at approximately 230C. It is sparingly soluble in water and methanol, slightly soluble in glacial acetic acid and ethanol, and practically insoluble in ether. The empirical formula of tamsulosin hydrochloride is C20H28N2O5S HCl. The molecular weight of tamsulosin hydrochloride is 444.98.

Each FLOMAX capsule for oral administration contains tamsulosin hydrochloride 0.4 mg, and the following inactive ingredients methacrylic acid copolymer dispersion, NF; microcrystalline cellulose, NF; triacetin, USP; calcium stearate, NF; talc, USP; FD&C blue No. 2; titanium dioxide; ferric oxide; gelatin, and trace amounts of black edible ink.

Analgin tablets are administered for the treatment of pains of various origin toothache, headache, arthralgia, neuralgia, myalgia, milder visceral pains, dysmenorrhea, as an antipyretic in the complex therapy of inflammatory diseases of upper respiratory tract, infectious diseases. Analgin solution for injection is used in cases of acute and severe pain after surgical operations or traumas; pains due to tumors; renal and biliary colics and high temperature unaffected by other drugs.

Hypersensitivity to metamizole and other pyrazolone derivatives; acute hepatic porphyria; inborn glucose-6-phosphate dehydrogenase deficiency; severe renal or hepatic diseases; hematologic diseases (aplastic anemia, leucopenia and agranulocytosis); first and last trimester of pregnancy. It should be avoided in lactating or pregnant women due to the lack of studies on its safety. Parenteral administration is contraindicated in children under 1 year.

Somatropin also commonly referred to as human growth hormone (HGH), is a hormone that is produced in the human body and excreted into the blood by the cells of the anterior pituitary gland. It is a single-chain protein that is composed of 191 amino acids with a molecular weight of approximately 22, 000 Daltons. It is used to treat growth failure in children and adults who lack natural growth hormone, and in those with chronic kidney failure, Noonan syndrome, Turner syndrome, short stature at birth with no catch-up growth, and other causes.Contact for detail.

Trazodone Hydrochloride used for the treatment of depression. However, it is sometimes prescribed as a sedative, and it also is used in combination with other drugs for the treatment of psychiatric conditions.

For the treatment of depression, the typical dose for adults is 150-600 mg per day. The initial dose usually is 150 mg per day. Trazodone is given in one or more divided doses, sometimes with the largest dose at night. Doses often are adjusted slowly upwards to find the optimal dose. Elderly patients and debilitated persons may need lower doses. Your physician will tell you your recommended dosage.

Selegiline hydrochloride is a levorotatory acetylenic derivative of phenethylamine. It is commonly referred to in the clinical and pharmacological literature as l- deprenyl.

The chemical name is (R)-(-)-N, -Dimethyl-N-2-propynylphenethylamine hydrochloride. It is a white to near white crystalline powder, freely soluble in water, chloroform, and methanol, and has a molecular weight of 223.75. The molecular formula is C13H17N.HCI. Each capsule, for oral administration contains 5 mg of Selegiline hydrochloride. In addition, each capsule contains the following inactive ingredients Anhydrous Lactose NF, Citric Acid Anhydrous USP, Microcrystalline Cellulose NF PH102, Stearic Acid NF and Talc USP. The capsule shell contains Gelatin NF, FD & C Blue #1 and Titanium Dioxide. The capsule logo ink Black SW-9008/SW-9009 contains the following inactive ingredients Ammonium Hydroxide; Black Iron Oxide, Bacteria Controlled EEC No. 172; n-Butyl NF; Ethyl Alcohol, Anhydrous, 200 Proof; Isopropyl Alcohol USP; Potassium Hydroxide NF; Propylene Glycol USP; Purified Water USP and Shellac NF.

An extremely poisonous white compound, KCN, used in the extraction of gold and silver from ores, in electroplating, and in photography, and as a fumigant and insecticide. (inorganic chemistry) The potassium salt of hydrocyanic acid, KCN; the colourless crystals are soluble in water, and it is extremely poisonous, and is used in electroplating, the extraction of gold and silver from their ores, and in photography.

vyvanse (lisdexamfetamine) is a central nervous system stimulant. It affects chemicals in the brain and nerves that contribute to hyperactivity and impulse control.

vyvanse is used to treat attention deficit hyperactivity disorder (adhd) in adults and in children who are at least 6 years old.

vyvanse may also be used for other purposes not listed in this medication guide.

do not use vyvanse if you have taken an mao inhibitor in the past 14 days. A dangerous drug interaction could occur. Mao inhibitors include isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, tranylcypromine, and others.

vyvanse is a drug of abuse and may be habit-forming. Keep track of the amount of medicine used from each new bottle. You should be aware if anyone is using your medicine improperly or without a prescription. Using this medication improperly can cause death or serious side effects on the heart.

you should not use vyvanse if you are allergic to lisdexamfetamine.

do not use vyvanse if you have taken an mao inhibitor in the past 14 days. A dangerous drug interaction could occur. Mao inhibitors include isocarboxazid, linezolid, methylene blue injection, phenelzine, rasagiline, selegiline, tranylcypromine, and others.

some stimulants have caused sudden death in people with serious heart problems or congenital heart defects. Tell your doctor if you have heart disease, heart rhythm disorder;

coronary artery disease (hardened arteries); or history of heart attack.

to make sure this medicine is safe for you, tell your doctor if you have high blood pressure;

peripheral vascular disease such as raynaud's syndrome;

a personal or family history of mental illness, psychotic disorder, bipolar illness, depression, or suicide attempt; or

if you take an antidepressant.

Phenethylamine, or phenylethylamine is an organic compound and a natural monoamine alkaloid, a trace amine, and also the name of a class of chemicals with many members that are well known for their psychoactive and stimulant effects.

Phenylethylamine functions as a neuromodulator or neurotransmitter in the mammalian central nervous system. It is biosynthesized from the amino acid L-phenylalanine by enzymatic decarboxylation via the enzyme aromatic L-amino acid decarboxylase. In addition to its presence in mammals, phenethylamine is found in many other organisms and foods, such as chocolate, especially after microbial fermentation. It is sold as a dietary supplement for purported mood and weight loss-related therapeutic benefits; however, orally ingested phenethylamine experiences extensive first-pass metabolism by monoamine oxidase B (MAO-B), which turns it into phenylacetic acid. This prevents significant concentrations from reaching the brain when taken in low doses.