PharmacyCodes



Daypro Alta en es it fr

Daypro Alta Brand names, Daypro Alta Analogs

Daypro Alta Brand Names Mixture

  • No information avaliable

Daypro Alta Chemical_Formula

C18H15NO3

Daypro Alta RX_link

http://www.rxlist.com/cgi/generic/oxaproz.htm

Daypro Alta fda sheet

Daypro_Alta FDA

Daypro Alta msds (material safety sheet)

Daypro_Alta MSDS

Daypro Alta Synthesis Reference

No information avaliable

Daypro Alta Molecular Weight

293.317 g/mol

Daypro Alta Melting Point

158 - 159 oC

Daypro Alta H2O Solubility

Insoluble

Daypro Alta State

Solid

Daypro Alta LogP

4.8

Daypro Alta Dosage Forms

Tablet

Daypro Alta Indication

Used to relieve the inflammation, swelling, stiffness, and joint pain associated with rheumatoid arthritis and osteoarthritis.

Daypro Alta Pharmacology

Oxaprozin is a nonsteroidal antiinflammatory drug (NSAID) with analgesic and antipyretic properties. Oxaprozin is used to treat rheumatoid arthritis, osteoarthritis, dysmenorrhea, and to alleviate moderate pain.

Daypro Alta Absorption

Oxaprozin is 95% absorbed after oral administration. Food may reduce the rate of absorption of oxaprozin, but the extent of absorption is unchanged. Antacids do not significantly affect the extent and rate of oxaprozin absorption.

Daypro Alta side effects and Toxicity

Oral, mouse: LD50 = 1210 mg/kg; Oral, rabbit: LD50 = 172 mg/kg; Oral, rat: LD50 = 4470 mg/kg

Daypro Alta Patient Information

Daypro, like other drugs of its class, can cause discomfort and, rarely, more serious side effects, such as gastrointestinal bleeding, which may result in hospitalization and even fatal outcomes. Although serious gastrointestinal tract ulcerations and bleeding can occur without warning symptoms, patients should be alert for the signs and symptoms of ulcerations and bleeding, and should ask for medical advice when observing any indicative sign or symptoms. Patients should be apprised of the importance of this follow-up.

Patients should report to their physicians the signs or symptoms of gastrointestinal ulceration or bleeding, skin rash, weight gain, or edema.

Patients should be informed of the warning signs and symptoms of hepatotoxicity (e.g., nausea, fatigue, lethargy, pruritus, jaundice, right upper quadrant tenderness, and “flu-like” symptoms). If these occur, patients should be instructed to stop therapy and seek immediate medical therapy.

Patients should also be instructed to seek immediate emergency help in the case of an anaphylactoid reaction.

In late pregnancy, as with other NSAIDs, Daypro should be avoided because it will cause premature closure of the ductus arteriosus.

Daypro Alta Organisms Affected

Humans and other mammals