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Penimox (Amoxicillin)
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Penimox

Penimox is acceptable for uncomplicated acute sinus infections; however, many doctors prescribe amoxicillin-clavulanate (Augmentin) as the first-line antibiotic to treat a possible bacterial infection of the sinuses. Penimox usually is effective against most strains of bacteria.

Other names for this medication:
Acimox, Alfamox, Almodan, Amoclen, Amopen, Amoram, Amoxi, Amoxicilina, Amoxicillin, Amoxicillinum, Amoxisol, Amoxypen, Amurol, Bimoxan, Clamoxyl, Flemoxin, Hidramox, Hydramox, Larotid, Lupimox, Moxicillin, Penamox, Polymox, Raylina, Reloxyl, Robamox, Servamox, Sintedix, Stacillin, Sumox, Tolodina, Velamox, Wymox

Similar Products:
Sumycin, Flagyl, Zithromax, Suprax, Terramycin, Myambutol, Levaquin, Amoxil

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Also known as: Amoxicillin

Description

Generic Penimox is a perfect remedy in struggle against infections caused by certain bacteria. It is also used with other medicines to treat Helicobacter pylori infection and ulcers of the small intestines. Generic Penimox acts by killing sensitive bacteria. It is a penicillin antibiotic. Generic Penimox only works against bacteria, it does not treat viral infections. Penimox is also known as Amoxicillin, Trimox, Actimoxi, Alphamox, AMK, Amoksibos, Amoxiclav Sandoz, Amoxin, Amoksiklav, Amoxibiotic, Amoxicilina, Apo-Amoxi, Bactox, Betalaktam, Cilamox, Curam, Dedoxil, Dispermox, Duomox, Enhancin, Gimalxina, Geramox, Hiconcil, Isimoxin. Generic name of Generic Penimox is Amoxicillin. Brand name of Generic Penimox is Penimox.

Dosage

Adults: 500 mg PO every 12 hours or 250 mg PO every 8 hours for mild/moderate infections and 875 mg PO every 12 hours or 500 mg PO every 8 hours for severe infections.

Infants 6 months and older, Children, and Adolescents: 80 to 90 mg/kg/day PO in divided doses every 12 hours is recommended by the American Academy of Pediatrics (AAP) as first-line therapy. Do not exceed 500 mg/dose if given every 8 hours or 875 mg/dose if given every 12 hours. AAP recommends a 10-day course for any child with severe disease and for all patients less than 2 years of age, regardless of severity. For children 2 to 5 years with mild to moderate disease, a 7-day course is acceptable. For children 6 years and older with mild to moderate disease, a 5- to 7-day course is acceptable. 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.

Infants 4 to 5 months: 80 to 90 mg/kg/day PO given in divided doses every 12 hours for 10 days was recommended by experts as first-line therapy in previous guidelines ; however, this age group is not addressed in the most current guidelines by the American Academy of Pediatrics (AAP). The FDA-approved dosage is 20 mg/kg/day PO in divided doses every 8 hours or 25 mg/kg/day PO in divided doses every 12 hours for mild to moderate infections and 40 mg/kg/day PO in divided doses every 8 hours or 45 mg/kg/day PO in divided doses every 12 hours for severe infections.

Infants 3 months and younger: 30 mg/kg/day PO given in divided doses every 12 hours is the general FDA-approved dosing. Young infants are less capable of responding to infection, and the clinical manifestations of infection can be subtle. Because of the increased risk for complications of an undiagnosed systemic infection, every young infant presenting with a fever should be carefully evaluated.

Overdose

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

Storage

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 Penimox 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

Geriatric. Based on manufacturer data, geriatric patients (above 65 years) do not respond differently to Penimox treatment than younger patients. However, a greater sensitivity to Penimox in elderly patients could not be ruled out. Penimox is known to be substantially excreted via the kidney. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection for elderly patients; renal function monitoring may be useful. The federal Omnibus Budget Reconciliation Act (OBRA) regulates medication use in residents of long-term care facilities. According to OBRA, use of antibiotics should be limited to confirmed or suspected bacterial infections. Antibiotics are non-selective and may result in the eradication of beneficial microorganisms while promoting the emergence of undesired ones, causing secondary infections such as oral thrush, colitis, or vaginitis. Any antibiotic may cause diarrhea, nausea, vomiting, anorexia, and hypersensitivity reactions.

Pregnancy. Penimox is classified in FDA pregnancy risk category B. Animal data reveal no teratogenic effects, however, there are no adequate and well-controlled studies in pregnant women. While Penimox should be used with caution in pregnancy, penicillins are usually considered safe during pregnancy when clearly needed.

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Non-Hodgkin lymphoma (NHL) is a malignancy etiologically linked to immunomodulatory exposures and disorders. Mapping of proteolytic and cyanogen bromide peptides from subunits of intestinal maltase-glucoamylase: evidence for significant homology. Psychotic patients had a significantly higher frequency of delusions in previous episodes. Acute renal failure from both ischemia and contrast are postulated to occur from free-radical injury. Combination phase I study of nedaplatin and gemcitabine for advanced non-small-cell lung cancer. Yields and aflatoxin levels were highly variable among sites although irrigated sites had higher yields than nonirrigated sites. The purpose of this clinical trial experiment was to compare the effects of the combination of dry needling (DN) and the muscle energy technique (MET) on the upper trapezius latent myofascial trigger point. Over the long term a large percentage of patients exhibit inadequately managed cardiovascular risk factors following an acute cardiac event. Limitation of the activated partial thromboplastin time as a monitoring method of the direct thrombin inhibitor argatroban. Therefore, a glyoxylyl-based labeling agent (e.g., radioactive tags, fluorescent probes, biotin) can be used to specifically modify a protein at its N-terminus.

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Total esophagectomy by stripping without thoracotomy in cancer of the pharynx, esophagus and cardia. Deletion of Ac150 alone had no effect on infectivity of the virus for either host. Molecular mimicry has been touted as a mean to develop new generation of vaccines to target carbohydrate antigens on pathogens and on tumor cells. A positive correlation between MAOA and SERT mRNA levels in the raphe nuclei area of the midbrain was shown. The analysis of patterns of co-occurrence and cotransmission of affective disorders and alcoholism in families may provide clues for understanding the excess comorbidity between these conditions in clinical settings and in the general population. After the first incubation at 4 degrees C for 4 days, 0.1 ml labeled PTH were added. Reduction surgery combined with intraarterial infusion chemotherapy was carried out in three patients with advanced primary liver cancer. Responding to tragic error: lessons from Foothills Medical Centre.

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We investigated the effects of water extracts of Ziziphus vulgaris L. Moral questions are raised that must be answered by nursing educators because the status quo in nursing practice, licensure, and education is morally unacceptable. Modification of both the soft and hard segments needs to be considered in order to maximize biodurability of both basic building blocks of the polyurethane. In EA experiments in which good analgesia was induced, plasma beta E was increased more (P less than 0.05) than in EA experiments in which poor analgesia was induced. Recent emphasis has focused on managing the malar region, specifically ptosis of the cheek pad. These three cases each had a positive epidemiological history suggestive of disease prior to ordering FA tests. Investigation of the effects of P2 purinoceptor ligands on the micturition reflex in female urethane-anaesthetized rats. Five of these children had a severe illness starting in the first months of life (range 20 days--4 months) and died within 4 months (range 19 days--10 months). By contrast, little is known about functions of IQGAP2 or IQGAP3. The optimal approach to the post-treatment management of patients with thoracic malignancies is a controversial topic.

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