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Topgesic (Ibuprofen)
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Topgesic

Topgesic is a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking your body's production of certain natural substances that cause inflammation. Topgesic is used to relieve pain from various conditions such as headache, dental pain, menstrual cramps, muscle aches, or arthritis.

Other names for this medication:
Addaprin, Advil, Arthophen, Artigesic, Brufen, Brutex, Buftiz, Codistar, Diclospas, Diplodac, Dolomed, Elbugesic, Gesic, Haltran, Ibrumac, Ibubid, Ibugin, Ibumol, Ibusynth, Ibuzen, Inflapen, Ipecee, Lobain, Maxofen, Menadol, Methoriv, Mortrin, Neurophen, Norswel, Nuren, Orthodex, Oxydin, Oxymark, Profon, Pyrofen, Rebufen, Robiflam, Rufen, Sugafen, Tizidal, Treza, Xtragesic

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Also known as: Ibuprofen

Description

Ibuprofen is a nonsteroidal anti-inflammatory drug (NSAID) used to treat mild to moderate pain, and helps to relieve symptoms of arthritis (osteoarthritis, rheumatoid arthritis, or juvenile arthritis), such as inflammation, swelling, stiffness, and joint pain. This medicine does not cure arthritis and will help you only as long as you continue to take it .

In addition, ibuprofen can be used to treat fever, menstrual cramps, and other conditions as determined by your doctor .

This medicine is available both over-the-counter (OTC) and with your doctor's prescription .

Dosage

This section provides information on the proper use of a number of products that contain ibuprofen. It may not be specific to Children's Topgesic Bubble Gum Flavor. Please read with care.

For safe and effective use of this medicine, do not take more of it, do not take it more often, and do not take it for a longer time than ordered by your doctor. Taking too much of this medicine may increase the chance of unwanted effects, especially in elderly patients .

When used for severe or continuing arthritis, this medicine must be taken regularly as ordered by your doctor in order for it to help you. This medicine usually begins to work within one week, but in severe cases up to two weeks or even longer may pass before you begin to feel better. Also, several weeks may pass before you feel the full effects of this medicine .

To lessen stomach upset, you may take this medicine with food or milk .

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 oral dosage form (tablets and suspension): For fever: Children over 2 years of age—Use and dose must be determined by your doctor. Children 6 months of age up to 2 years—Dose is based on body weight and body temperature, and must be determined by your doctor. For fever lower than 102.5 °F (39.2 °C), the dose usually is 5 milligrams (mg) per kilogram (kg) (about 2.2 mg per pound) of body weight. For higher fever, the dose usually is 10 mg per kg (about 4.5 mg per pound) of body weight. The medicine may be given every six to eight hours, as needed, up to 40 mg per kg per day. Infants younger than 6 months of age—Use and dose must be determined by your doctor . For menstrual cramps: Adults—400 milligrams (mg) every four hours, as needed. Children—Use and dose must be determined by your doctor . For mild to moderate pain: Adults and teenagers—400 milligrams (mg) every four to six hours, as needed. Children over 6 months of age—Dose is based on body weight and must be determined by your doctor. The dose usually is 10 milligrams (mg) per kilogram (kg) of body weight every six to eight hours, as needed, up to 40 mg per kg per day. Infants younger than 6 months of age—Use and dose must be determined by your doctor . For osteoarthritis and rheumatoid arthritis: Adults and teenagers—1200 milligrams (mg) up to 3200 mg per day divided into three or four equal doses. Children—Dose is based on body weight and must be determined by your doctor. The dose usually is 30 milligrams (mg) to 40 mg per kilogram (kg) of body weight per day, divided into three or four doses. Infants younger than 6 months of age—Use and dose must be determined by your doctor .

Overdose

If you overdose Topgesic and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Topgesic overdosage: uncontrolled eye movements, blue color around lips, mouth, and nose, slow breathing, feeling lightheaded.

Storage

Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.

Ask your healthcare professional how you should dispose of any medicine you do not use.

Keep out of the reach of children.

Do not keep outdated medicine or medicine no longer needed.

Detailed Topgesic Childrens dosage information

Side effects

The most common side effects associated with Topgesic 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

Appropriate studies performed to date have not demonstrated geriatrics-specific problems that would limit the usefulness of ibuprofen in the elderly. However, elderly patients are more likely to have age-related kidney problems, which may require adjustment of dosage in patients receiving ibuprofen .

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Overall, there was no significant association of the VDR gene polymorphisms with familial prostate cancer risk in the cases and control subjects. The aim of this study is to comparatively elucidate the underlying molecular pathways and clinicopathological criteria in schistosomal bladder tumor (SBT) versus non-schistosomal bladder tumor (NSBT). In order to determine whether the testicular degeneration observed is peripherally or centrally mediated, we investigated effects of i.c.v. Recombinant HPV16 L1 pentamers assemble in vitro into capsid-like structures, and truncation of ten N-terminal residues leads to a homogeneous preparation of 12-pentamer, icosahedral particles. Initiatives in the preregistration year (general clinical training). With respect to the similar conditions used in finite-difference or finite-volume implementations, some corrections are needed to compensate the isothermal compressible nature of standard lattice Boltzmann methods for fluid flow. It was also found that not only the erythrocyte aggregation, but also the strength of the aggregates formed were increased: this correlated well with the disease gravity. Interferon beta1a therapy changes lipoprotein metabolism in patients with multiple sclerosis. Substituent effects on xenon binding affinity and solution behavior of water-soluble cryptophanes. Improvement on this standard of practice continues to be elusive, in large part because of the effects of associated radiation.

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In this study, we analyzed the presence of mutations at codons 12 and 13 of the K-ras gene in 165 Danish women with ovarian tumours, including 138 invasive ovarian cancers and 27 borderline ovarian tumours, using a restriction fragment length polymorphism-polymerase chain reaction technique and evaluated whether such alterations were associated with the clinicopathological parameters of the patients and survival. The impact of joint responses of devices in an airport security system. The right upper lobe was most frequently involved, followed by the left upper, right lower and left lower lobe. Carboxen/poly(dimethylsiloxane) was the most sensitive to small molecules and acids. A review of the uses and limitations of tocainide--a class IB antiarrhythmic agent. Herein, we report a new case of 1-bromopropane-induced neurotoxicity. We found that disassembly of the Golgi complex by brefeldin A treatment resulted in partial inhibition of cholesterol transport while completely blocking HA transport. For FLU, under the same conditions, t(1/2) values were 1.9-2.3 and 3.6-6.4 days, respectively. Here we review recent methods in chemical biology and optogenetics for controlling the nuclear localization of proteins of interest inside living cells.

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During fasting, migrating complexes were present in the segment, but were replaced by intermittent spike activity during chenodeoxycholate without and with ricinoleic acid perfusion. The entire covering process appears to be random and poorly coordinated until very late in the 4-day cycle. Contemporary techniques for arthroscopic knotless repair offer possible advantages over traditional arthroscopically tied knots. The implementation of a clinical practice guideline is essential to standardize the diagnosis, treatment and prognosis of this rhythm disturbance. The ROC methodology uses ordinal dominance theory and bootstrap resampling to evaluate A(z) and confidence intervals in simple as well as paired data analyses. This commentary addresses the New Zealand study (case report) of a fatal pulmonary embolism (PE) associated with oral contraceptive (OC) use by L. We determined the sequence of the IDH1 gene and the related IDH2 gene in 445 central nervous system (CNS) tumors and 494 non-CNS tumors. Although for a constant number of modes the reconstruction error is a little higher for the KPCA-based statistical model, it produces a statistical model with substantially better specificity than PCA- and ICA-based models. After analysis, we photobleached the PE molecules by irradiating the sample with blue light. As compared to control, ADP-induced, thromboformation and behaviour, exogenous paf-acether causes a large, dense platelet thrombus, invaded and surrounded by numerous leukocytes, spreading widely over the adjoining, vacuolized, endothelium.

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Recipients of the donor cells were (BALB/c x C3H)F1 and (BALB/c x C57)F1 hybrids. It is unclear whether these reactions represent an atypical response to clenbuterol or another unidentified contaminant. Further large scale trials are warranted to evaluate the relationship between platelet activation markers and outcome in stroke patients under different anti-platelet therapies, and to clarify optimal treatment. The aim of this study was to assess the effect of parental 5,10-methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms (677C/T and 1298A/C) on response to single-dose methotrexate (MTX) treatment in tubal ectopic pregnancy (TEP). In a large number of genetic association studies in humans, the nonconservative LEPR Q223R allele has been inconsistently associated with adiposity. Appetitive-based learning in rats: lack of effect of chronic exposure to fluoride. This history has produced a nested pattern of genetic structure that is inconsistent with the existence of independently evolving biological races. In vivo release of 3H-GABA synthesized from 3H-Glutamine in the substantia nigra and the pallido entopeduncular nuclei in the cat. By using the oxygen radical absorbance capacity (ORAC) assay, the oxygen radical scavenging ability of the SWCNT antioxidants is nearly 40 times greater than that of the radioprotective dendritic fullerene, DF-1. These studies identify a FDA approved drug as a potential treatment for NF2 and delineate the mechanism of action in NF2-null Schwann cells.

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Double knockdown of ERK1 and ERK2 did not improve the effects of single knockdowns of ERK1 and ERK2 in either cell types. We found a statistically significant decrease in total protein levels in samples transported by PTS. Investigation by coronary arteriography in experimental and clinical practice. Regional cerebral blood flow determination, following post-angiographic intracarotid injection of 133Xenon, was performed in 11 patients with transient (T.I.A. Resuscitation and transfusion management in trauma patients: emerging concepts. Results suggest that patients who undergo an arthroplasty following urgent or emergent FNFs have inferior outcomes to those receiving an arthroplasty for a diagnosis of arthritis. Revascularization of the left ventricle by double internal mammary artery implant. This study was undertaken to determine the efficacy of percutaneous vertebroplasty in treating patients with painful compression fractures of the thoracic and lumbar vertebrae that contain intraosseous vacuum phenomena. Two of these proteins were identified as alpha-fetoprotein and alpha-macrofetoprotein. Skin sensitization potential of low molecular weight chemicals was assessed by analyzing peptide-conjugate formation.

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