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Aurogra (Sildenafil)
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Aurogra

Aurogra is an oral medication intended for the treatment of erection problems in men. It is offered to buy online in the form of diamond-shaped blue tablets for oral administration containing 100 mg Sildenafil citrate. Aurogra is a Generic version of Viagra manufactured by Aurochem.

Other names for this medication:
Caverta, Cenforce, Intagra, Kamagra, Nizagara, Penegra, Revatio, Silagra, Sildenafil, Sildenafila, Sildenafilo, Sildenafilum, Sildigra, Suhagra, Veega, Zenegra

Similar Products:
Glucophage, Aldara, Seroquel, Persantine, Vasotec, Detrol, Daklinza

Also known as: Sildenafil

Description

Aurogra is produced by Aurochem Labs. This drug is available in the form of a pill and must only be ingested orally. The active ingredient Sildenafil Citrate is absorbed into the blood stream and starts to act within 30 to 60 minutes. The function of the medication is to inhibit the PDE5 (phosphodiesterase) enzyme which is located in the region of the penis. It relaxes the smooth muscles in the blood vessels of the penis, increases blood flow in this area and thus provides a hard erection. The effect of the medication can last up to 4 hours, allowing you to choose the most appropriate time for you and your partner. Aurogra doesn't protect you or your partner from sexually transmitted diseases (including HIV) or from pregnancy. Aurogra is not intended for the treatment of women or children.

Dosage

Aurogra tablet should be taken orally with a full glass of water on an empty stomach, 30-60 minutes before sexual intercourse. Dosage depends on the general health of the patient. You should only take Aurogra when it is suitable for you and your partner. Aurogra must not be taken more than once a day. In order to achieve the quickest results avoid alcohol, high-fat meals and grapefruit juice. In elderly patients, an initial dose of 50 mg once a day is recommended. Use Aurogra only when needed. Do not take a double dose of Aurogra.

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 at room temperature between 15 and 30 degrees C (59 and 86 degrees F) and away from excess moisture and heat. 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 Aurogra 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 Aurogra if you are allergic to Aurogra's components. Do not take Aurogra if you are also using organic nitrates, nitrate drug for chest pain or heart condition (e.g., nitroglycerin, isosorbide dinitrate, and isosorbide mononitrate), nitrates as amyl nitrate or nitrite ("poppers"). Do not take Aurogra if you take other medication to treat erectile dysfunction, pulmonary arterial hypertension, such as riociguat (Adempas). Do not take Aurogra in you are taking erythromycin, medicines called alpha-blockers, ketoconazole, itraconazole (Sporanox or Nizoral), ritonavir (Norvir) or indinavir (Crixivan). Try not to consume alcohol while using Aurogra, as it can lower your blood pressure, causing dizziness and rapid heart rate (tachycardia). Do not drive or operate machinery while taking the medication. Contact you doctor or health care professional right away if the erection lasts longer than 4 hours or if it becomes painful. Aurogra does not protect you and your partner from sexually transmitted diseases and pregnancy. Aurogra can be dangerous for children and women.

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Metabolic profiles have been shown to provide prognostic information in patients with heart failure (HF). The third conclusion is that mesenchyme which is already differentiating into hand structures at the time of transplantation (hand plate of paddle-shaped upper-arm blastema, and oldest carpal blastema) upon dedifferentiation can be induced to form more proximal structures as well. At 0.5 h, cyclic AMP response element (CRE)-binding protein (CREB) and binding was slightly elevated, whereas activator protein- 2 (AP-2) and specificity protein 1 (Sp1) binding were not affected. Therefore, we have cloned human SAC1 (hSAC1), show that it behaves similar to ySac1p in terms of substrate specificity, demonstrate that the endogenous protein localizes to the ER and Golgi, and identify for the first time members of the coatomer I (COPI) complex as interaction partners of hSAC1. Determination of five macrolide antibiotic residues in eggs using liquid chromatography/electrospray ionization tandem mass spectrometry. Intrathecal adjuvants are often administered during this procedure to provide significant analgesia, but they may also have bothersome side effects. We found that AAV vectors are highly efficient for gene transfer to the mouse skin, displaying an exquisite tropism for the panniculus carnosus by using the beta-galactosidase activity assay.

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Unraveling genes and pathways influenced by H-prune PDE overexpression: a model to study cellular motility. The time period of monitoring for embolic signals may be reduced without loss of clinical relevant information when signal frequency is low or already high during the reduced monitoring period, but it should be prolonged to maximally an hour at signal numbers within a medium range. We therefore suggest that a pronounced moult-breeding overlap is not a typical strategy used by long-distance migrants to adjust to the short breeding season at northern latitudes. Studies with a stromal cell line (MC3T3-G2/PA6) and fibroblasts (3T3) suggested that glucocorticoids act directly on the stromal cells that produce tenascin. To determine if there are distinct symptom patterns in women with IBS and endometriosis, and to determine the response of these women to a low FODMAP diet in comparison to those with IBS alone. In an overview format for primary care physicians and psychiatrists, the metabolism and drug interactions in the context of antiretroviral therapy are presented for the following drugs of abuse: alcohol, benzodiazepines, cocaine, GHB (liquid X), ketamine (special K), LSD (acid), MDMA (Ecstasy), opiates, PCP (angel dust), and THC (marijuana). Phase III refers to transporter-mediated elimination of drug and/or metabolites from body normally via liver, gut, kidney, or lung. Although CRCIOM was a rare event in the investigated patient population, our results emphasize that pre-treatment dental therapy and primary preventive measures (including oral hygiene instructions) can be improved. Vulvar pain with some relationship to sexual intercourse appears to be a significant problem among Ghanaian women.

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Determinant factors for development of adult T cell leukemia (ATL) and tropical spastic paraparesis (TSP) are complex and treatment outcomes have been disappointing. Therefore, MCP-1-mediated monocyte infiltration is essential in the development of restenotic changes as well as atherosclerosis progression. The purpose of this study was to analyze cartilage degeneration in knees after total medial meniscectomy, transplantation of fresh-frozen meniscus allograft, and Achilles tendon allograft. The subcellular element distribution and the uptake and distribution of (33)P was analyzed in non-mycorrhizal and mycorrhizal roots of these plants and compared with plants kept constantly under normal light conditions (control what is bactrim drug classification plants). Alcohol drinking was associated with HCC and interacted with HBsAg positivity. Antituberculous chemotherapy was started and his chest X-ray findings were improved. At high matrix densities, there is considerable heterogeneity in the diffusion of the fluid particles.

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