Deflam
Deflam Brand names, Deflam Analogs
Deflam Brand Names Mixture
- No information avaliable
Deflam Chemical_Formula
Deflam RX_link
Deflam fda sheet
Deflam msds (material safety sheet)
Deflam Synthesis Reference
Deflam Molecular Weight
Deflam Melting Point
Deflam H2O Solubility
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Deflam LogP
Deflam Dosage Forms
Deflam Indication
Deflam Pharmacology
Deflam Absorption
Deflam side effects and Toxicity
Deflam 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.
