Medicines

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Lamivudine (2',3'-dideoxy-3'-thiacytidine, commonly called 3TC) is a potent nucleoside analog reverse transcriptase inhibitor (nRTI). It is marketed by GlaxoSmithKline with the brand names Zeffix, Heptovir, Epivir, and Epivir-HBV. Lamivudine has been used for treatment of chronic hepatitis B at a lower dose than for treatment of HIV. It improves the seroconversion of e-antigen positive hepatitis B and also improves histology staging of the liver. Long term use of lamivudine unfortunately leads to emergence of a resistant hepatitis B virus (YMDD) mutant. Despite this, lamivudine is still used widely as it is well tolerated.

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As a quality-centric organization of this industry, we are engaged in offering a wide array of Prosteride 1. The offered product is processed according to the medical industry norms by utilizing pioneering procedures and supreme grade of chemical compounds. Our given product is extremely recognized for its accurate composition. Thisproduct is properly checked on different specified parameters in order to supply flawless range from our side.

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NICOTINE 2MG CHEWING GUMS

TYPICAL USAGE:  withdrawal.

SIDE EFFECTS: Hyperglycemia, increased blood lactate, hypoinsulinemia, epileptic seizures, sweating, respiratory arrest, tremor, hyperpnea, palpitation, sweating, tremor, faintness, paresthesias, pallor.

DRUG INTERACTION: Nicotine is known to interact with other drugs like insulin, papaverine (HCl), , theophylline. These interactions are sometimes beneficial and sometimes may pose threats to life. Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.

MECHANISM OF ACTION: Nicotine is a stimulant drug that acts as an agonist at nicotinic acetylcholine receptors. These are ionotropic receptors composed up of five homomeric or heteromeric subunits. In the brain, nicotine binds to nicotinic acetylcholine receptors on dopaminergic neurons in the cortico-limbic pathways. This causes the channel to open and allow conductance of multiple cations including sodium, calcium, and potassium. This leads to depolarization, which activates voltage-gated calcium channels and allows more calcium to enter the axon terminal. Calcium stimulates vesicle trafficking towards the plasma membrane and the release of dopamine into the synapse. Dopamine binding to its receptors is responsible the euphoric and addictive properties of nicotine. Nicotine also binds to nicotinic acetylcholine receptors on the chromaffin cells in the adrenal medulla. Binding opens the ion channel allowing influx of sodium, causing depolarization of the cell, which activates voltage-gated calcium channels. Calcium triggers the release of from intracellular vesicles into the bloodstream, which causes vasoconstriction, increased blood pressure, increased heart rate, and increased blood sugar.

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NICOTINE 2MG CHEWING GUMS

TYPICAL USAGE:  withdrawal.

SIDE EFFECTS: Hyperglycemia, increased blood lactate, hypoinsulinemia, epileptic seizures, sweating, respiratory arrest, tremor, hyperpnea, palpitation, sweating, tremor, faintness, paresthesias, pallor.

DRUG INTERACTION: Nicotine is known to interact with other drugs like insulin, papaverine (HCl), , theophylline. These interactions are sometimes beneficial and sometimes may pose threats to life. Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.

MECHANISM OF ACTION: Nicotine is a stimulant drug that acts as an agonist at nicotinic acetylcholine receptors. These are ionotropic receptors composed up of five homomeric or heteromeric subunits. In the brain, nicotine binds to nicotinic acetylcholine receptors on dopaminergic neurons in the cortico-limbic pathways. This causes the channel to open and allow conductance of multiple cations including sodium, calcium, and potassium. This leads to depolarization, which activates voltage-gated calcium channels and allows more calcium to enter the axon terminal. Calcium stimulates vesicle trafficking towards the plasma membrane and the release of dopamine into the synapse. Dopamine binding to its receptors is responsible the euphoric and addictive properties of nicotine. Nicotine also binds to nicotinic acetylcholine receptors on the chromaffin cells in the adrenal medulla. Binding opens the ion channel allowing influx of sodium, causing depolarization of the cell, which activates voltage-gated calcium channels. Calcium triggers the release of from intracellular vesicles into the bloodstream, which causes vasoconstriction, increased blood pressure, increased heart rate, and increased blood sugar. 

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We are actively involved in offering a vast range of Generic Drugs. After consuming best quality chemical compound and updated technology, the offered indinavir tablet is processed under hygienic conditions by vendor’s practiced professionals. We are providing this indinavir tablet in frequent packaging options as according to the needs. Clientele can benefit this indinavir tablet from us at very nominal rates.

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Clemastine, also known as meclastin, is an antihistamine drug. Unlike loratadine or fexofenadine, clemastine is a sedating antihistamine, however it exhibits fewer side effects than most of the widely used antihistamines. Clemastine is also classified as an antipruritic (i.e. it stops itching).

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Please contact us via email at for the detailed product and price list.We assure you for the quality supply and error free services from our side..you can get in touch email

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Ovral L Tablet (LEVONORGESTREL + ETHINYL ESTRADIOL)
LEVONORGESTREL + ETHINYL ESTRADIOL

• Ovral L - Product Information Ovral L is a monophasic, low dose combination of Levonorgestrel and Ethinylestradiol Tablets I.P. used to prevent pregnancy. Each combined oral contraceptive (COC) tablet contains 150 µg of Levonorgestrel I.P. and 30 µg of Ethinyl estradiol.
• Active Pharmaceutical Ingredient in Ovral LThe active pharmaceutical ingredients in Ovral L are levonorgestrel I.P. 150 µg (0.15 mg) and ethinyl estradiol I.P. 30 µg (0.03 mg).
• Uses of Ovral LOvral L is used to prevent pregnancy.
• Dosage and Administration Take one pill of Ovral L daily at the same time for 21 consecutive days. Start taking the next pack of 21 tablets after 7 days.
• How to start Ovral L
• If you have not used an oral contraceptive in the previous month:
• Take the first tablet on day 1 of your natural cycle, i.e. on the first day of your period.
• If you start on day 2-7, you will have to use for the first seven days an additional nonhormonal method of birth control (such as ).
• If you have used before another oral contraceptive:
• Start taking Ovral L on the day after the last tablet of your previous pill, latest on the day following the usual tablet-free (or inactive tablet) interval.
• Changing from a progestin only method (progestin-only pill, injection, implant)
• You may switch any day from the progestin-only pill and begin Ovral L the next day. Start Ovral L on the day of an implant removal or, if you used an injection before, the day the next injection would be due.
• It is advised to use an additional protection for the first 7 days.
• Do not start taking Ovral L before 28 days after delivery.
• Drug Class and Mechanism Ovral L belongs to the group of oral contraceptives.
• Ovral L acts by suppression of gonadotropins. Although the primary mechanism of this action is inhibition of ovulation, other alterations include changes in the cervical mucus (which increases the difficulty of spermS entry into the uterus) and in the endometrium (which reduces the likelihood of implantation).

Missed Dose

• If you miss one tablet, but not more than 12 hours have passed, take the tablet as soon as you remember. Take the next tablet at the usual time.

• If you miss one tablet, and more than 12 hours have passed, or if you missed more than one tablet, your protection against pregnancy may be reduced.. The last missed tablet should be taken as soon as you remember, even if this means taking two tablets in one day. Subsequent tablets should be taken at the usual time. In addition, a nonhormonal back-up method of birth control should be used for the next seven days.

• If two tablets in a row are missed in week 1 or week 2 of a pack, two tablets should be taken on the day you remember, and two tablets the next day. Subsequent tablets should be taken at the usual time. In addition, a nonhormonal back-up method of birth control ( such as ) should be used for the seven days after tablets are missed.

• If two active tablets in a row are missed in week 3 of a pack, or if three or more tablets in a row are missed in weeks 1-3 of a pack, discard the rest of the packet and start a new packet the same day. Use additional methods to prevent pregnancy.
• Storage Of Ovral L TabletsStore Ovral L at room temperature away from heat and moisture. Keep out of reach of children and pets. Store in a cool place.

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Budesonide is a glucocorticoid steroid for the treatment of asthma, non-infectious rhinitis (including hay fever and other allergies), and for treatment and prevention of nasal polyposis. Additionally, it is used for Crohn''s disease (inflammatory bowel disease).
 It is marketed by AstraZeneca as a nasal inhalant under the brand name Rhinocort (in Denmark, as Rhinosol), as an oral inhalant under the brand name Pulmicort, and as either an enema or a modified release oral capsule under the brand name Entocort. It is also sold in combination with (Oxis) in a single inhaler, under the brand name Symbicort. In Brazil it''s marketed by Eurofarma under the brand name Noex.

PharmacodynamicsPharmacokinetics 

Budesonide controls the rate of protein synthesis, depresses the migration of polymorphonuclear leukocytes, fibroblasts, reverses capillary permeability and lysosomal stabilisation at the cellular level to prevent or control inflammation.
Absorption: Rapid and almost complete after oral admin but has poor systemic availability.
Metabolism: Undergoes first-pass metabolism.

Budesonide Indications / Budesonide Uses

Information Not Available

Budesonide Adverse Reactions / Budesonide Side Effects

Loss of skin collagen and SC atrophy; local hypopigmentation of deeply pigmented skin; dryness, irritation, epistaxis, rarely ulceration or perforation of the nasal septum; smell and taste disturbances; hoarseness and candidiasis of the mouth or throat.

 

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Duloxetine is a selective serotonin and norepinephrine reuptake inhibitor antidepressant (SSNRI). Duloxetine affects chemicals in the brain that may be unbalanced in people with depression. Duloxetine is used to treat major depressive disorder in adults

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ZOSTAVAX® is a live attenuated virus vaccine indicated for prevention of herpes zoster (shingles) in individuals 50 years of age and older. Limitations of Use of ZOSTAVAX: • ZOSTAVAX is not indicated for the treatment of zoster or postherpetic neuralgia (PHN)

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Oxcarb Tablets is an anticonvulsant and mood stabilizing drug, used primarily in the treatment of epilepsy. It is also used to treat anxiety and mood disorders, and benign motor tics. Oxcarbazepine is a structural derivative of carbamazepine, with a ketone in place of the carbon-carbon double bond on the dibenzazepine ring. This difference helps reduce the impact on the liver of metabolizing the drug, and also prevents the serious forms of anemia or agranulocytosis occasionally associated with carbamazepine. Aside from this reduction in side effects, it is thought to have the same mechanism as carbamazepine - sodium channel inhibition (presumed to be the main mechanism of action) - and is generally used to treat the same conditions. Oxcarbazepine has recently been found to be associated with a greater enhancement in mood and reduction in anxiety symptoms than other drugs employed to treat epilepsy.
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International Brand Name: Eldoquin/Solaquin Brand Name: Eukroma

Hydroquinone decreases the formation of melanin in the skin. Melanin is the pigment in skin that gives it a brown color.

Hydroquinone topical is used to lighten areas of darkened skin such as freckles, age spots, chloasma, and melasma.

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

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Eukroma (Hydroquinone) is a skin-bleaching agent that is used to lighten areas of darkened skin such as freckles, chloasma (also known as melasma), age spots, and acne scars.

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Ezetimibe is used along with a low cholesterol/low fat diet and exercise to help lower cholesterol in the blood. Ezetimibe may be used alone or with other drugs (such as "statins" or fibrates). Ezetimibe works by reducing the amount of cholesterol your body absorbs from your diet.

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Clotrimazole is an antifungal medication commonly used in the treatment of fungal infections of both humans and animals such as vaginal yeast infections, oral thrush, and ringworm. It is also used to treat athlete's foot and jock itch.

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We do have availability of AMOXYCILLIN, we have availability of 250 mg and 500 mg. It is used to treat bacterial infections, such as chest infections (including pneumonia) and dental abscesses. It can also be used together with other antibiotics and medicines to treat stomach ulcers. It's often prescribed for children, to treat ear infections and chest infections.

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Osteofos tablets 70mg are used to treat osteoporosis, to reduce the risk of vertebral and hip fractures in men and postmenopausal women, and to prevent osteoporosis developing in postmenopausal women who are at risk. Osteoporosis is the loss of bone mass resulting in brittle bones which can fracture more easily and is often associated with lack of oestrogen in postmenopausal women or following treatment with a corticosteroid, an anti-inflammatory steroid that can cause bone loss. Osteofos tablets 70mg are also used to treat Paget''s disease of bone in men and women, in which the normal mechanism of bone turnover is faulty and bone structure becomes abnormal causing weakness. Osteofos tablets 70mg help to strengthen the bone structure making them less likely to fracture. 

Osteofos tablets 70mg contain alendronate, which is a bisphosphonate; a synthetic chemical similar to the naturally occurring mineral in bone called pyrophosphate that mediates bone turnover, a normal part of bone remodelling, which is a dynamic process that allows bones to grow and repair. Alendronate acts directly on bone and binds to hydroxyapatite (the scaffolding of bone architecture), specifically at the site of bone resorption (the process for removal of old bone tissue), and inhibits the action of bone cells called osteoclasts that are responsible for bone resorption. Alendronate has no effect on osteoblast cells that are responsible for bone formation (laying down of new bone tissue). Osteofos tablets 70mg change the balance of bone turnover so that bone breakdown is reduced relative to bone building, which increases bone mass, making bones stronger and more resistant to fracture, which can be painful and cause loss of height if the fracture occurs in the spine. Although alendronate in Osteofos tablets 70mg begin working on bone turnover immediately, it may take several months before measurable effects on bone mass may be seen. 

Osteofos tablets are available from Inhouse Pharmacy in 2 doses:

• Osteofos 70mg tablets for once weekly administration
• Osteofos 10mg tablets for once daily administration

Osteofos tablets 70mg contain alendronate, which is a bisphosphonate; a synthetic chemical similar to the naturally occurring mineral in bone called pyrophosphate that mediates bone turnover, a normal part of bone remodelling, which is a dynamic process that allows bones to grow and repair. This process of bone turnover is hormonally controlled and is increased by oestrogen and decreased by corticosteroids. During menopause, oestrogen production slows down and this increases risk of osteoporosis, the loss of bone mass, in menopausal women. Aging also causes bones to weaken due to loss of bone density, so that men are also susceptible to osteoporosis. Also low levels of can cause loss of bone density. Long-term use of corticosteroid medication (an anti-inflammatory steroid) can also cause bone loss. Osteofos tablets 70mg are used to treat men and postmenopausal women with osteoporosis, and to prevent osteoporosis in pre-menopausal women who are know to be at risk of osteoporosis; also to treat and prevent corticosteroid-induced osteoporosis in men, pre-menopausal women and postmenopausal women receiving oestrogen. Osteofos tablets 70mg increase bone density and reduce the risk of vertebral and hip fractures, which can be painful and cause loss of height if the fracture occurs in the spine.

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Descriptions. Infliximab injection is used in adults to treat Crohn disease, ulcerative colitis, rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, and chronic severe plaque psoriasis. It is also used in children to treat Crohn disease and ulcerative colitis

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Crestor (rosuvastatin) belongs to a a group of drugs called HMG CoA reductase inhibitors, or "statins." Rosuvastatin is used together with diet to lower blood levels of "bad" cholesterol (low-density lipoprotein, or LDL), to increase levels of "good" cholesterol (high-density lipoprotein, or HDL), and to lower

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Ofloxacin is a fluoroquinolone antibiotic considered to be a second-generation fluoroquinolone. Floxin (branded version) had been discontinued by the manufacturer, in the United States, effective June 18, 2009, though generic equivalents continue to be available.
Ofloxacin is a racemic mixture, which consists of 50% levofloxacin (the biologically active component) and 50% of its “mirror image” or enantiomer dextrofloxacin. When levofloxacin disks were not available in early clinical trials, a 5-pg Floxin (ofloxacin –floxacin) disk was substituted. The U.S. Food and Drug Administration (FDA) medical reviewers considered the two drugs to be one and the same and hence interchangeable.

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Methotrexate, abbreviated MTX and formerly known as amethopterin, is an antimetabolite and antifolate drug used in treatment of cancer and autoimmune diseases. It acts by inhibiting the metabolism of folic acid. Methotrexate began to replace the more powerful and toxic antifolate aminopterin starting in the 1950s, and the two should not be confused with each other.

PharmacodynamicsPharmacokinetics 

Methotrexate is a folic acid antagonist that inhibits DNA synthesis. It irreversibly binds to dihydrofolate reductase, inhibiting the formation of reduced folates, and thymidylate synthetase, resulting in inhibition of purine and thymidylic acid synthesis.

 

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Olmesartan is an angiotensin II receptor blocker (ARB). It works by blocking a substance in the body that causes the blood vessels to tighten. As a result, olmesartan relaxes the blood vessels. This lowers blood pressure and increases the supply of blood and oxygen to the heart

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INDIVAN in combination with antiretroviral agents is indicated for the treatment of HIV infection.

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Fexofenadine (Allegra, Telfast, Fastofen, Tilfur) is an antihistamine drug used in the treatment of hayfever and similar allergy symptoms. It was developed as a successor of and alternative to (brand names include Triludan and Seldane), an antihistamine with potentially serious contraindications. Fexofenadine, like other second and third-generation antihistamines, does not readily cross the blood-brain barrier, and so causes less drowsiness than first-generation histamine-receptor antagonists. It works by being an antagonist to the H1 receptor.

It has been described as both second-generation and third-generation.

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With our hard-earned experience of this industry, we offer a vast range of Fluoxetine Capsules. Our provided Pilocar eye drop is accurately processed using finest chemical compounds, ingredients and updated techniques by vendor’s proficient professionals. We reassure our customers that this Pilocar eye drop is quality tested on specified parameters which is predefined. Along with that, our valuable clients can take this Pilocar eye drop, as per their needs, at highly affordable rates.

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Imatinib is a drug used to treat certain types of cancer. It is currently marketed by Novartis as Gleevec (USA) or Glivec (Europe/Australia) as its mesylate salt, imatinib mesilate (INN) (formerly called STI-571). It is used in treating chronic myelogenous leukemia (CML), gastrointestinal stromal tumors (GISTs) and other cancers. It is the first member of a new class of agents that act by specifically inhibiting a certain enzyme that is characteristic of a particular cancer cell, rather than non-specifically inhibiting and killing all rapidly dividing cells. In CML, the enzyme tyrosine kinase is stuck in the "on" position. Imatinib binds to the site of tyrosine kinase activity, and prevents its activity.

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Enbrel is used to treat rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis, and to prevent joint damage caused by these conditions. Enbrel is also used to treat polyarticular juvenile idiopathic arthritis in children who are at least 2 years old