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Asmapax (Theophylline)
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Asmapax

Asmapax has two distinct actions in the airways of patients with reversible obstruction; smooth muscle relaxation and suppression of the response of the airways to stimuli.

Other names for this medication:
Alergin, Ambrolite, Asmapan, Asmapax, Asmasule, Asthasol, Asthimo, Asthmino, Asthom, Azofen, Biodryl, Biryth, Bronchophyl, Broncophyl, Bronkasma, Bronkfylin, Bronkoplus, Curamol, Delin, Deriphyllin, Efelin, Lontif, Mediphylline, Phylin, Phylobid, Phyloday, Relasmin, Respiphylline, Salbeto, Salorex, Solebeta, Sphylin, Tedral, Theobric, Theobus, Theoclear, Theoday, Theophylline, Theoresp, Theosalbid, Theosol, Theostan, Theotabllin, Theovent, Ventiphylline, Ventirex, Winphyllin, Zeriphyllin, Zeriphylline

Similar Products:
Furadantin, Keflex, Persantine, Plavix, Astelin, Clomid, Mysoline, Cyphoden, Encold, Dynapres, Zonda, Alpress, Tamdura, Pioglit, Brethmol, Simol, Precose,

Also known as: Theophylline

Description

Asmapax is an HMG-CoA reductase inhibitor. Asmapax is used to: reduce the risk of heart attack, stroke, and death due to coronary heart disease; reduce the risk of heart attack, stroke, blood vessel blockage, or chest pain caused by angina; low high cholesterol and triglycerides; increase high-density lipoprotein (HDL, "good") cholesterol levels. Asmapax is also known as Imvastatin, Simlup, Simcardis, Ranzolont, Simvador. Asmapax works by reducing the production of certain fatty substances in the body, including cholesterol. Generic name of Asmapax is Simvastatin. Brand name of Asmapax is Asmapax.

Dosage

Usual Adult Dose for Chronic Hepatitis C:

400 mg orally once a day Recommended Regimen and Duration of Therapy: -Genotype 1 or 4: Sofosbuvir, peginterferon alfa, and ribavirin for 12 weeks -Genotype 2: Sofosbuvir and ribavirin for 12 weeks -Genotype 3: Sofosbuvir and ribavirin for 24 weeks -Hepatocellular carcinoma awaiting liver transplantation: Sofosbuvir and ribavirin for up to 48 weeks or until liver transplantation (whichever occurs first) Comments: -Genotype 1, 4: This regimen is recommended for therapy-naive patients without cirrhosis or with compensated cirrhosis (Child-Pugh A). -Genotype 2, 3: Both regimens are recommended for therapy-naive and therapy-experienced patients without cirrhosis or with compensated cirrhosis (Child-Pugh A). -Therapy-experienced patients have failed an interferon-based regimen (with or without ribavirin). -The dose recommendations for genotype 1, 2, 3, or 4 should be followed for HCV/HIV-1-coinfected patients. -The manufacturer product information should be consulted for ribavirin tablet dose recommendations; with genotype 1 or 4, the manufacturer product information for peginterferon alfa should also be consulted for dose recommendations. -Sofosbuvir and ribavirin for 24 weeks can be considered for patients with genotype 1 infection who cannot use an interferon-based regimen; treatment decision should be guided by benefit/risk assessment for the individual patient. -The regimen for patients with hepatocellular carcinoma awaiting liver transplantation is recommended to prevent posttransplant HCV reinfection. Use: As a part of a combination antiviral treatment regimen, for the treatment of chronic HCV infection -In combination with pegylated interferon and ribavirin: For genotype 1 or 4 infection without cirrhosis or with compensated cirrhosis -In combination with ribavirin: For genotype 2 or 3 infection without cirrhosis or with compensated cirrhosis

Usual Pediatric Dose for Chronic Hepatitis C:

3 years or older: -Weight less than 17 kg: 150 mg orally once a day -Weight 17 to less than 35 kg: 200 mg orally once a day -Weight at least 35 kg: 400 mg orally once a day Recommended Regimen and Duration of Therapy: -Genotype 2: Sofosbuvir and ribavirin for 12 weeks -Genotype 3: Sofosbuvir and ribavirin for 24 weeks -Hepatocellular carcinoma awaiting liver transplantation: Sofosbuvir and ribavirin for up to 48 weeks or until liver transplantation (whichever occurs first) Comments: -Both regimens are recommended for therapy-naive and therapy-experienced patients without cirrhosis or with compensated cirrhosis (Child-Pugh A). -Therapy-experienced patients have failed an interferon-based regimen (with or without ribavirin). -The manufacturer product information should be consulted for ribavirin dose recommendations. -The same dose recommendations should be followed for HCV/HIV-1-coinfected patients. -The regimen for patients with hepatocellular carcinoma awaiting liver transplantation is recommended to prevent posttransplant HCV reinfection. Use: In combination with ribavirin, for the treatment of chronic HCV genotype 2 or 3 infection in patients without cirrhosis or with compensated cirrhosis

Detailed Asmapax dosage information

Overdose

If an overdose occurs and you are not feeling well, you should seek emergency medical attention or contact your healthcare provider immediately.

Storage

Store below 25 degrees C (77 degrees F) away from moisture, light and heat. Keep container tightly closed. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Asmapax are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

You should not take Asmapax if you are allergic to alendronate, or if you have:

low levels of calcium in your blood (hypocalcemia); or problems with the muscles in your esophagus (the tube that connects your mouth and stomach).

Do not take Asmapax if you cannot sit upright or stand for at least 30 minutes. Asmapax can cause serious problems in the stomach or esophagus. You must stay upright for at least 30 minutes after taking this medicine.

To make sure this medicine is safe for you, tell your doctor if you have ever had:

trouble swallowing; problems with your stomach or digestion; low levels of calcium in your blood; a dental problem (you may need a dental exam before you begin taking Asmapax); kidney disease; or any condition that makes it hard for your body to absorb nutrients from food (malabsorption).

In rare cases, this medicine may cause bone loss (osteonecrosis) in the jaw. Symptoms include jaw pain or numbness, red or swollen gums, loose teeth, or slow healing after dental work. The longer you use Asmapax, the more likely you are to develop this condition.

Osteonecrosis of the jaw may be more likely if you have cancer or received chemotherapy, radiation, or steroids. Other risk factors include blood clotting disorders, anemia (low red blood cells), and a pre-existing dental problem.

Asmapax has also been reported to cause fractures, or broken bones, in the large bones of the leg. Tell your doctor if you have any leg or groin pain while using Asmapax.

Talk with your doctor about the risks and benefits of using this medication.

It is not known whether Asmapax will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant. Stop using the medicine and tell your doctor right away if you become pregnant.

It is not known whether alendronate passes into breast milk or if it could harm a nursing baby. Ask your doctor about any risk.

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Overexpression in neuroblastoma cells of a paxillin LD4 deletion mutant inhibited lamellipodia formation in response to insulin-like growth fac- tor-1. Case records of one-hundred patients operated on for centrally prolapsed lumbar intervertebral disc were analyzed for establishing of typical clinical symptom complex. Our study adds evidence to the superiority of the fibrillation technique over intermittent cross-clamping of the aorta, among non-cardioplegic techniques, in terms of neurological protection. Swabs from the cervix and placental membranes were cultured for aerobic and anaerobic organisms. The hMCMs bound to the nuclei in the presence of ATP were released by digestion with nucleases, suggesting that they are chromatin-associated. The use of these needles is the most effective method available for anaesthetists to reduce the incidence of post dural puncture headache. It was found that all transgenic tobacco and potato plants expressed the N protein in the leaves, whereas transgenic potato plants are able to significantly express the viral proteins also in the tubers and roots. In a plastic (VP 1527) model of the sagittal section of a foot skeleton the distribution of stressing under load has been visualized in photographs of the isochromes as seen in the polarized light. The authors retrospectively studied 58 patients (58 eyes) who underwent vitreous examination.

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Biochemical experiments indicate that Bdf1 competes with the Sir2 deacetylase for binding to acetylated histone H4. Distraction of XIAP consequently liberates caspase-3 to autocatalytically process into active p17. The EWMA control chart: properties and comparison with other quality-control procedures by computer simulation. The high patient acceptability makes transvaginal hydrolaparoscopy suitable as an early stage procedure in the investigation of infertility and as a repeat or second look procedure. Analysis of process parameters affecting spray-dried oily core nanocapsules using factorial design. However, the presence of increased levels of connective tissue in muscular dystrophies, such as Duchenne muscular dystrophy (DMD), may affect the efficiency of this process. Discharge planning proposed rule focuses on patient preferences.

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Regulation of pancreatic islet gene expression in mouse islets by pregnancy. The repeated bouts of dynamic exercise with training also expose the temperature regulatory system to increased body temperatures and attendant demands for increased heat loss. The structure of limacine, limacusine and cuspidaline, new phenolic bisbenzylisoquinoline bases. A mammalian two-hybrid system was used to assay the protein-protein interactions. Currently, there is an urgent need for further clinical studies regarding the criteria for recommending AS, the criteria for reclassification on AS, and the schedule for AS. Using renal carcinoma and prostate carcinoma cell lines, we investigated the concept of targeting and killing multidrug resistant cells in urogenital cancers. Erosion of the surrounding bone, including the cribriform plate, resulted in an intracranial component in the four cases. All fetuses found to have an isolated congenital clubfoot over a 9-year period were retrospectively identified. Aortic Pseudoaneurysm Secondary to Mediastinitis due to Esophageal Perforation. There was no significant difference in transfusion, conversion to open surgery albendazole 400 mg brand name , overall complications, severe complications, pancreatic fistula, severe pancreatic fistula, ICU stay, total cost, and 30-day mortality between the two groups.

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