drug
SODIUM CHLORIDE
updated 4mo agoby LIEBEL-FLARSHEIM
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Trials studying SODIUM CHLORIDE
- phase2Clinical Trial of Omalizumab for Allergen Sensitized and Exposed Individuals With COPD
- phase2A Study of BEBT-701 in Patients With Mild to Moderate Hypertension and Elevated Low-Density Lipoprotein Cholesterol（LDL-C）
- phase2Phase II Clinical Study of HRS-9563 in Patients With Mild to Moderate Hypertension
- phase2Randomised Treatment of Acute Pancreatitis With Infliximab: Double-blind, Placebo-controlled, Multi-centre Trial (RAPID-I)
- phase2A Clinical Study Evaluating the Efficacy and Safety of HRS-7249 in Treating Patients With Hyperlipidemia
- phase2Interest of a Targeted Therapy for the Treatment of a Severe Form of Hypersensitivity to Drug (DRESS Syndrome)
- phase2A Study of SRSD107 in Participants With Chronic Coronary and/or Peripheral Arterial Disease
- phase2A Study of PRL3-zumab in Neovascular Age-related Macular Degeneration (nAMD)
News(8)
- Sodium Chloride Flush Recall: Spectra Medical Removes Sodium Chloride Injection USP AmpulesSpectra Medical Devices is removing Sodium Chloride Flush products that were manufactured by Huons Co,. Ltd.fda_medwatch · 1d ago
- Epidural Kit Correction: Medical Action Industries Issues Correction for Epidural Kits Containing Spectra Medical Devices Lidocaine AmpulesMedical Action Industries is correcting epidural kits containing recalled Huons Co. sodium chloride ampules.fda_medwatch · 9d ago
- B. Braun Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container Due to the Presence of Particulate MatterFOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Con…fda_recalls · 16d ago
- Early Alert: Convenience Kit Issue from AVID MedicalAVID Medical is correcting convenience kits containing recalled Huons Co. sodium chloride ampules.fda_medwatch · 17d ago
- Baxter Issues Voluntary Nationwide Recall for Two Lots of 0.9% Sodium Chloride Injection Due to Potential Presence of Particulate MatterFOR IMMEDIATE RELEASE – AUG. 25, 2026 – DEERFIELD, Ill., Baxter International Inc. (NYSE:BAX) is voluntarily recalling two lots of 0.9% Sodium Chloride Injection due to the potential presence of pa…fda_medwatch · 24d ago
- Early Alert: Epidural Kit Issue from Medical Action IndustriesMedical Action Industries is correcting epidural kits containing recalled Huons Co. sodium chloride ampules.fda_medwatch · 29d ago
- Early Alert: Convenience Kit Issue from Becton DickinsonBD is correcting convenience kits and procedural trays containing recalled Huons Co. sodium chloride ampulesfda_medwatch · 1mo ago
- Convenience Kit Correction: Arrow International Issues Correction for Convenience Kits Containing Recalled Huons Lidocaine and Bupivacaine and SalineSaline, Lidocaine and Bupivacaine from affected convenience kits should not be used.fda_medwatch · 2mo ago
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