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Asthimo (Theophylline)
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Asthimo

Asthimo has two distinct actions in the airways of patients with reversible obstruction; smooth muscle relaxation (i.e., bronchodilation) and suppression of the response of the airways to stimuli (i.e., non-bronchodilator prophylactic effects).

Other names for this medication:
Asmapan, Asmapax, Asmasule, Asthasol, Asthocap, Asthom, Bronkasma, Bronkfylin, Bronkoplus, Deriphyllin, Durasalyn, Efelin, Etophylate, Etophylline, Graphyllin, Lontif, Onimar, Pherin, Phyloday, Salonimar, Salorex, Salphylate, Salphylline, Sivoxol, Sulbex, Theoday, Theoder, Theophylline, Theopin, Theoresp, Theoriv, Theosal, Theotabllin, Unicontin, Ventil, Ventiphylline, Zeriphylline

Similar Products:
Cycrin, Xenical, Duricef, Sildigra, Hydrea, Nolvadex, Sinequan, Prandin

Also known as: Theophylline

Description

Nevirapine is used in combination with other medicines for the treatment of the infection caused by human immunodeficiency virus (HIV). HIV is the virus that causes acquired immune deficiency syndrome (AIDS).

Nevirapine is a non-nucleoside reverse transcriptase inhibitor (NNRTI). It works by lowering the amount of HIV in the blood.

Nevirapine will not cure HIV infection or AIDS, however, it helps keep HIV from reproducing and appears to slow down the destruction of the immune system. This may help delay the development of problems that usually result from AIDS or HIV disease. Nevirapine will not keep you from spreading HIV to other people. People who receive this medicine may continue to have some of the problems usually related to AIDS or HIV disease.

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

Dosage

This section provides information on the proper use of a number of products that contain imiquimod. It may not be specific to Asthimo. Please read with care.

It is very important that you use this medicine only as directed by your doctor. Do not use more of it, do not use it more often, and do not use it for a longer time than your doctor ordered. To do so may cause unwanted side effects or skin irritation.

This medicine is for use on the skin only. Do not get it in your eyes, nose, mouth, vagina, or anus. Do not use it on skin areas that have cuts, scrapes, or burns. If it does get on these areas, rinse it off right away with water.

This medicine comes with a patient information leaflet. Read and follow the instructions in the leaflet carefully. Ask your doctor if you have any questions.

This medicine should only be used for skin conditions that your doctor is treating. Check with your doctor before using it for other conditions, especially if you think that a skin infection may be present. This medicine should not be used to treat certain kinds of skin infections or conditions, such as severe burns.

If you are using the Zyclara® cream pump for the first time, prime it by pressing the top of the pump until the cream appears.

To use the cream:

Wash your hands with soap and water before and after using the medicine. Use one or two packets or actuations of the pump of cream for each dose as directed by your doctor. Apply a thin layer to the affected area of the skin just before bedtime. Rub it in gently. Allow the medicine to stay on the treated skin for 8 hours (for actinic keratosis or basal cell carcinoma) or 6 to 10 hours (for genital warts). Do not take a bath, swim, or get the treated area wet during this time. After the right amount of time has passed, wash the treated area with mild soap and water. Men who are not circumcised and are treating genital warts under the foreskin should retract the foreskin and clean the area daily. Do not bandage or otherwise wrap the skin being treated, unless directed to do so by your doctor. Materials that are not airtight, such as cotton gauze or cotton underwear, may be used if needed. Throw out any unused cream from the single-dose packet.

Use only the brand of this medicine that your doctor prescribed. Different brands may not work the same way.

Do not use this medicine together with any other products containing imiquimod in the same treatment area. This may increase risk for more serious side effects.

The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

For topical dosage form (cream): For actinic keratosis: Adults—If you use Zyclara®, apply a thin film to the affected area of skin once a day at bedtime for 2 weeks. Your doctor will repeat the treatment after you go 2 weeks without medicine. If you use Asthimo®, apply a thin film to the affected area of skin once a day at bedtime 2 times per week for 16 weeks. Your doctor will tell you which days are best during the week. Children—Use and dose must be determined by your doctor. For skin cancer: Adults—Apply a thin film to the affected area of skin once a day at bedtime 5 times per week for 6 weeks. Your doctor will tell you which days are best during the week. Children—Use and dose must be determined by your doctor. For external warts: Adults and children 12 years of age and older—If you use Zyclara®, apply a thin film to the wart once a day at bedtime for up to 8 weeks or until the wart is gone. If you use Asthimo®, apply a thin film to the wart once a day at bedtime 3 times per week. Your doctor will tell you which days are best during the week. Use the medicine until the wart is gone, but for no longer than 16 weeks. Children younger than 12 years of age—Use and dose must be determined by your doctor.

Overdose

If you overdose Generic Asthimo and you don't feel good you should visit your doctor or health care provider immediately.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture 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 Asthimo 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

Do not take Asthimo if you are allergic to Asthimo ingredients. Do not take Asthimo if you are in a state of diabetic ketoacidosis. Asthimo is ineffective and possibly harmful in treatment of type 1 diabetes. Do not take Asthimo if you have congestive heart failure or heart disease, fluid retention, a history of bladder cancer, heart attack, stroke, liver disease, certain eye problems (macular edema), or polycystic ovary syndrome. Asthimo is not to be used in people with blood in their urine when the cause of this is unknown. Avoid drinking alcohol. It lowers blood sugar level and may interfere with your diabetes treatment. Be careful with Asthimo if you are pregnant, planning to become pregnant, or breastfeeding. Do not use Asthimo in treatment of children under 18 years old. Asthimo may increase the risk of bone fracture in women (usually in the upper arm, hand, or foot). Asthimo can cause changes in the menstrual cycle (promote ovulation) and increase the risk of becoming pregnant. Do not take Asthimo for longer than recommended. Taking Asthimo for more than 1 year may increase your risk of developing bladder cancer.

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Comprehensive characterization of these transcripts is envisaged to augment our understanding on the genes involved in testicular functions and sustenance of a viable paternal genome during pre- and post- fertilization events and early stages of development. Synthesis and biological activity of two metabolites of 1-methyl-5-(1-methylethyl)-2-nitro-1 H-imidazole, an antiprotozoal agent. DNA epitope vaccine containing complement component C3d enhances anti-amyloid-beta antibody production and polarizes the immune response towards a Th2 phenotype. With intravenous administration of capsaicin, a tight glottal closure, decreases in blood pressure, and bradycardia were observed. MRP2 may be predominantly involved in the telmisartan pharmacokinetics in humans. Polyurethanes are polymeric plastics that were first used as substitutes for traditional polymers suspected to release volatile organic hazardous substances. This review describes the strategy for the development of multifunctional dendrimeric and hyperbranched polymers, collectively named dendritic polymers, aiming at their application as drug and gene delivery systems.

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Cortical actin filaments in untreated cells were replaced by stress fibers after TGFbeta treatment, but peripheral actin aggregates were seen in vitreous-treated cells. The interaction of graphene with biomolecules has a variety of useful applications. The role of cyclic AMP in the regulation of smooth muscle cell contraction in the uterus. Thus, constitutive activation due to c-Kit mutations is involved in the pathogenesis of several forms of cancer, e.g. speciosus for the first time and compounds of 7-10 were obtained from C. Confirmatory phase II trials often attempt to estimate median survival in addition to response proportion, since this is the primary endpoint for most phase III cancer studies. Pinpoint papular variant of polymorphous light eruption: clinical and pathological correlation. To study insulin resistance and parental obesity as predictors of improvement in weight status in obese children and adolescents undergoing therapeutic life change intervention (TLC).

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Working memory and decision-making biases in young adults with a family history of alcoholism: studies from the Oklahoma family health patterns project. A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD). Specifically, NO appears to affect some aspects of neuronal tumour progression, particularly the chemoresistance phenotype, through inhibition of MYC activity and expression of a large set of ATP binding cassette transporters. Triple-phase helical CT scans can distinguish several types of atypical small HHs. Amino acids in the TM4-TM5 loop of Na,K-ATPase are important for biosynthesis.

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The involvement of NO on the increase of lung and intestinal microvascular permeability and the lymph effects on HUVEC detachment were also studied. The aims of this study were to describe the circumstances in which MSS was offered to pregnant women and their reasons for undertaking it. Consequently, as STS is widely distributed throughout the entire body, it has a substantial influence on hormone-dependent cancer mitogenesis. With regard to change in diagnostic criteria for ML, the geographical distribution of ML death rates by subtype shows variation over the last 20 years. Use of FMOC-protected (2)H(3)-Leu in the automated oligopeptide synthesis provided the required isotopomers for use as internal standard. A 26-year-old Zimbabwean woman commenced emtricitabine, tenofovir and efavirenz (Atripla) in December 2011.

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Quantum yields and molar absorptivities were measured for unconjugated IRDye 800CW and IRDye 800CW-tilmanocept (800CW-tilmanocept) preparations at 0.7, 1.5, 2.3, 2.9, and 3.8 dyes per tilmanocept. Next, Dolores Malaspina, MD, reviews the neurodevelopmental and neurodegenerative components of schizophrenia. Instead, Syk activation induces the tumor suppressor B-lymphocyte-induced maturation protein-1 (Blimp-1), which interferes with the expression of the antiapoptotic protein Bcl-2. Both label-free and amplified approaches can be used throughout feasibility testing and ultimately in the final assay, providing a robust platform for biopolymer analysis over a very broad dynamic range. The connection between dimer stability, monomer alpha helix unwinding, and salt bridge presence is investigated. By contrast, alcohol-caffeine combinations did not significantly alter breath alcohol levels, heart rate or subject-rated drug effects, relative to the effects of the drugs alone. This reaffirms the role of BRCA1 as caretaker in preserving genomic integrity. When studying these interventions, the safety of staff and patients should be included as on outcome measure. Creating selective pressure on reliable antibiotics by inappropriately reducing their doses will undoubtedly challenge these agents and may destroy entire drug classes with similar mechanisms of action or resistance.

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Severe periportal fibrosis is not an inevitable consequence of infection with Schistosoma mansoni. Fourty days after CRT, he suddenly complained severe pain in the left chest and abdomen, and vomiting. The extended multidomain solution structures of the complement protein Crry and its chimeric conjugate Crry-Ig by scattering, analytical ultracentrifugation and constrained modelling: implications for function and therapy. Mandibular coronoid process in parathyroid hormone-related protein-deficient mice shows ectopic cartilage formation accompanied by abnormal bone modeling. In response to: Burkhart P.V., Svavarsdottir E.K., Rayens M.K., Oakley M.G., Orlygsdottir B.

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Trochanteric rotational osteotomy for osteonecrosis of the femoral head. We performed a systematic review of randomized controlled trials evaluating the efficacy of interventions targeting PF among ICU survivors. Diagnosis and prognosis of behavior disorder associated with organic brain disease in children. Our results provide insight into the molecular anatomy of senescence pathways and its regulation by HPV on-coproteins. One assumption of this model is that single-headed SmM is fully active regardless of phosphorylation. Programs with space-time methods were selected for dose of prevacid inclusion, limiting our review to ClusterSeer, SaTScan, GeoSurveillance and the Surveillance package for R. Pegylated interferon and ribavirin-induced depression in chronic hepatitis C: role of personality.

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Epidermal morphogenesis: the transcriptional program of human keratinocytes during stratification. Breast and prostate carcinomas are among those cancers that respond to Hsp90 inhibitors in animal xenograft models and in early studies in patients. A conformational change in the benzeneboronic acid-alpha-chymotrypsin complex. Experiments were performed in precollicular decerebrate cats to investigate whether proprioceptive volleys originating from Golgi tendon organs and muscle spindles may activate supraspinal descending inhibitory mechanisms. Furthermore, we also discuss their potential to influence other key components of the inflammatory response to infection. Association between offspring birth weight and atherosclerosis in middle aged men and women: British Regional Heart Study. A 3-year-old Thoroughbred colt was presented to the University Veterinary Centre Camden for evaluation of ataxia. The Omega Cohort Study was a longitudinal study of HIV-negative MSM aged 16 years or older and living in Montreal. We propose that genetically caused complement disorders should be considered when confronted with severe cases of B. To examine the influence of a selective noradrenaline reuptake inhibitor (SNRI) on the exercise-induced increase in circulating brain-derived neurotrophic factor (BDNF).

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Observations on the transabdominal approach in excision of diseased intervertebral disks. The NR(bright) cells expressed Sf1 and the more differentiated adrenal cortical genes, including Cyp11a1, Cyp11b1, and Cyp11b2, whereas the NR(dim) cells expressed Sf1 but not the more differentiated adrenal cortical genes. However, medications applied topically and as needed may be underreported. This paper presents a full state feedback adaptive dynamic inversion method for uncertain systems that depend nonlinearly upon the control input. We suggest that, despite the absence of regularly mapped functions in rat V1 (e.g. In addition, we started a prospective study in 2007, using LMWH therapy to prevent thromboplastic and atherosclerotic effects of the metabolic syndrome. Neurotensin administered intracisternally inhibits responsiveness of mice to noxious stimuli. Lovastatin, which binds under the conformationally mobile C-terminal alpha-helix of the I domain, inhibited binding to ICAM-1 by alphaLbeta2 with wild-type, but not locked-open I domains. An introduction to the types of genetic association studies is followed by a discussion of their potential use in risk assessment for age-related macular degeneration and type 2 diabetes mellitus.

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