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FDA FAERS Case Reports for Betamethasone/Calcipotriene Combination (4 Cases)
FDA FAERS Case Reports for Betamethasone/Calcipotriene Combination (4 Cases)
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Original Request: 4 (four) cases was found during FAERS screening: 1) Case id: 24790848, suspect product active ingredient: Betamethasone Dipropionate\Calcipotriene, Reactions: Drug Ineffective. 2) Case id: 24790823, suspect product active ingredient: Betamethasone Dipropionate\Calcipotriene, Reactions: Blood Cholesterol Increased;Product Prescribing Issue;Hypertension;Drug Ineffective. 3) Case id: 24547956, suspect product active ingredient: Betamethasone\Calcipotriene, Reactions: Product Quality Issue;Application Site Discomfort;Application Site Pain. 4) Case id: 24547955, suspect product active ingredient: Betamethasone\Calcipotriene, Reactions: Pain;Off Label Use;Product Container Issue etc
Tags: Pharma, FAERS, 2025
Tags: Pharma, FAERS, 2025
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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