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1 Οκτ 2024 · Recalls, Market Withdrawals, & Safety Alerts. The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products. Not all ...
- Enforcement Reports
Recall data in the Enforcement Report can be accessed...
- Industry Guidance For Recalls
Initiation of Voluntary Recalls Under 21 CFR Part 7, Subpart...
- Major Product Recalls
Recalls associated with Almark’s recall of hard-boiled egg...
- Archive for Recalls, Market Withdrawals & Safety Alerts
The Recalls, Market Withdrawals & Safety Alerts are...
- Enforcement Reports
Recall the patient after a minimum of 48 hours and remove the pellet. Complete the endodontic treatment and restore. Formocresol pulpotomy in primary teeth: Isolate the tooth with a rubber dam.
Buckley introduced formocresol in 1904, which is the most commonly used medicament for pulpotomy. The success rate of formocresol pulpotomy ranged from 70 to 98%. 6 Histological findings observed with the use of formocresol ranged from slight inflammation to total degeneration and necrotic changes.
3 Μαΐ 2023 · The current paper aimed to review the properties of formocresol and concerns regarding its safety as a pulpotomy medicament for primary teeth. With reference to the context of the recently...
Formocresol. Formocresol has been used in dentistry for over 100 years, and for vital pulpotomy in primary teeth for over 80 years. Its efficacy has been extensively studied, with clinical success rates ranging from 70% to 100%, making it the standard against which newer techniques are compared.
1 Ιουλ 2008 · The children were recalled 1, 6, 9, 12, 18, and 24 months for clinical and radiographic evaluation and were designed as single-blinded randomized clinical trial.
With a mouse lymphoma cell line, cultured human fibroblasts, and a series of formocresol dilutions similar to clinical doses, these authors found that formocresol did not produce detectable DNA damage and should not be considered genotoxic.