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Amoxypen (Amoxicillin)

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Amoxypen is a widely-used antibiotic drug. It belongs to the penicillin group of drugs and is prescribed to treat certain infections that are caused by bacteria. It can also be used alongside other medications to treat stomach ulcers caused by H. pylori infection.

Other names for this medication:
Alfamox, Aloxyn, Amoclen, Amoram, Amoxi, Amoxicilina, Amoxicillin, Amoxicillinum, Amoxiline, Amoxisol, Amurol, Bimoxan, Cipmox, Clamoxyl, Flemoxin, Flemoxon, Galenamox, Gimalxina, Hidramox, Hydramox, Lupimox, Moxicillin, Penamox, Penimox, Raylina, Reloxyl, Stacillin, Tolodina, Utimox, Velamox

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Also known as: Amoxicillin


Amoxypen is one of the best forms of antibiotic available today. It is used to treat infections caused by certain bacteria, including: infections of the ear, nose, and throat (pneumonia, bronchitis); infections of the genitourinary tract; infections of the skin and skin structure; infections of the lower respiratory tract; gonorrhea, acute uncomplicated (ano-genital and urethral infections) in male and females.

Amoxypen is also used before some surgery or dental work to prevent infection. It is also used in combination with other medications to eliminate H. pylori, a bacteria that causes ulcers. Amoxypen may also be used for other purposes not listed here.

Amoxypen acts by inhibiting the synthesis of bacterial cell wall and stopping the growth of bacteria.

Amoxypen is available in capsules.

Amoxypen is usually taken every 8 hours (three times a day). It can be taken with or without food.

The chewable tablets should be crushed or chewed thoroughly before they are swallowed. The tablets and capsules should be swallowed whole and taken with a full glass of water.

Take Amoxypen exactly as directed. Do not take more or less Amoxypen or take it more often than prescribed by your doctor. Do not stop taking Amoxypen without talking to your doctor. To clear up your infection completely, continue taking Amoxypen for the full course of treatment even if you feel better in a few days. Stopping Amoxypen too soon may cause bacteria to become resistant to antibiotics.


Adults: 1 g PO once daily or 500 mg PO twice daily for 10 days. The American Heart Association (AHA) recommends extended-release Amoxypen as an alternative to penicillin V for rheumatic fever prophylaxis.

Infants, Children, and Adolescents: 25 mg/kg/dose (Max: 500 mg/dose) PO twice daily for 10 days is recommended by the Infectious Diseases Society of America (IDSA). Alternatively, 50 mg/kg/dose PO once daily (Max: 1 g/dose) for 10 days is recommended by The American Heart Association (AHA) as an alternative to penicillin V. For ear/nose/throat infections in general, the FDA-approved dosage is 20 mg/kg/day PO in divided doses every 8 hours (Max: 250 mg/dose) or 25 mg/kg/day PO in divided doses every 12 hours (Max: 500 mg/dose) for mild to moderate infections and 40 mg/kg/day PO in divided doses every 8 hours (Max: 500 mg/dose) or 45 mg/kg/day PO in divided doses every 12 hours (Max: 875 mg/dose) for severe infections.


In case of overdosage, discontinue medication, treat symptomatically, and institute supportive measures as required. If the overdosage is very recent and there is no contraindication, an attempt at emesis or other means of removal of drug from the stomach may be performed. A prospective study of 51 pediatric patients at a poison-control center suggested that overdosages of less than 250 mg/kg of Amoxypen are not associated with significant clinical symptoms and do not require gastric emptying.

Interstitial nephritis resulting in oliguric renal failure has been reported in a small number of patients after overdosage with Amoxypen.

Crystalluria, in some cases leading to renal failure, has also been reported after Amoxypen overdosage in adult and pediatric patients. In case of overdosage, adequate fluid intake and diuresis should be maintained to reduce the risk of Amoxypen crystalluria.

Renal impairment appears to be reversible with cessation of drug administration. High blood levels may occur more readily in patients with impaired renal function because of decreased renal clearance of Amoxypen. Amoxypen may be removed from circulation by hemodialysis.


Store between 20 and 25 degrees C (68 and 77 degrees F) away from moisture and heat. Keep bottle closed tightly. 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 Amoxypen 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.


Dialysis, renal failure, renal impairment.

Use Amoxypen with caution in patients with renal impairment as the drug is substantially eliminated via renal mechanisms. Adjust dosage intervals in patients with CrCl 30 mL/min and in patients with renal failure. Dosage adjustments are also recommended for patients receiving dialysis. Do not use the extended release tablet in patients with CrCl 30 mL/min.

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Metastatic disease of bone and treatment of pathological fractures. Interestingly, disruption of Pten, an upstream regulator of TSC1/TSC2, in the same cells, does not lead to PKD seemingly due to limited activation of mTORC1, suggesting that PTEN may not be a major upstream regulator of TSC/mTORC1 during early postnatal kidney development. Noncompliance with NASPGHAN-ESPGHAN practice guidelines for GER in Europe: is there a point?. We propose that dynamic knowledge representation of gut HPI with agent-based modeling will aid in the investigation of the pathogenesis of gut-derived sepsis. Impaired rhodanese expression is associated with increased whole cell reactive oxygen species as well as higher mitochondrial superoxide production and predicts mortality in hemodialysis patients. The DNA extracts were used to amplify 16S ribosomal fragments, which were subsequently analyzed by denaturing gradient gel electrophoresis (DGGE). During the MFC operation, the hydrophilic and acidic fractions were more readily degraded, compared to the neutral fractions. Although they cannot be considered fully specific to OCD, they are more important in explaining OCD symptoms than general distress and harm-related beliefs, and they are also better indicators of OCD severity than HA.

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Our findings challenge the view that absence of paraproteinemia is a peculiar characteristic of APPM and raise once more the question of its relationship to the discrete papular form of lichen myxedematosus. Rotational angiography was performed from the hepatic artery for evaluation of the tumor feeding vessels. Among various concepts about systems theory the evaluation by Riedl seems to be the most efficient to explain medical procedures. No study has proven that routine screening reduces the mortality from prostate cancer. Pim-1 expression was investigated in a series of human leukemia cell lines with immunohistochemistry and flow cytometry. Size-dependent phase stability of a molecular floxin otic suspension nanocrystal: a proxy for investigating the early stages of crystallization. Interleukin-15 treatment improves glucose homeostasis and insulin sensitivity in obese mice. However, biochemical methods cannot effectively distinguish between pathogenic and non-pathogenic xanthomonads. We report the effects of hippocampal and non-hippocampal temporal-lobe dysfunction on verbal fluency performance. Coexpression of cdk2/cdc2 and retinoblastoma gene products in colorectal cancer.

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The concentrations of LH, total estrogens, and pregnanediol 3 alpha-glucuronide (PdG) were flagyl antibiotic and c diff determined by specific radioimmunoassays on daily overnight urine samples obtained in 13 menstrual cycles of six adult female chimpanzees during the periods of increasing, maximal, and decreasing tumescence of the perineal sex skin. In vitro experiments have shown sorafenib to be metabolized by the drug-metabolizing enzyme cytochrome P450 3A4 (CYP3A4) and glucuronosyltransferase (UGT1A9). Only a marginally significant sex difference is found along the entire length of the map and results from one interval, between D9S58 and D9S59, that displays an excess of female recombination. Several different sizes of double-strand probes were compared by dot-blot hybridization. Dental trauma could be largely classified into three groups: Hard tissue injuries, pulp injuries and periodontal tissue injuries. Clonal origin of Philadelphia chromosome negative cells with trisomy 8 appearing during the course of alpha-interferon therapy for Ph positive chronic myelocytic leukemia. 5-Substituted 3-mercapto-4H-1,2,4-triazoles as a potential thyrostaticagent. Shape matters when engineering mesoporous silica-based nanomedicines. Through small interfering RNA-mediated knockdown, chemical inhibition, expression of a dominant-negative mutant, and/or reexpression in knockout cells, we found PIM1 activity to be essential for proper CXCR4 surface expression and migration of cells toward a CXCL12 gradient. Effect of human immunodeficiency virus on the outcome of hepatitis C virus infection.

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