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Zoll LifeVest 4000 Wearable Cardioverter Defibrillator: FDA Safety Communication – Potential Lack of Treatment (Shock) Delivery Due to Device Failure

Murilo Freitas - 14:40, 16 de enero de 2018763
Failure to immediately replace the device after Message Code 102 appears may result in serious patient harm or death of the patient because the device may fail to deliver therapy when needed.

https://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm592710.htm

 
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INVIMA Alerta: Agua Estéril para Inyección Ampoulepack contaminada

Murilo Freitas - 13:32, 16 de enero de 20181,277

Bogota , 15 enero de 2018

Alerta No. 88

Invima alerta sobre el producto: «Agua Estéril para Inyección Ampoulepack x 10 mL lote 70307 y Agua Estéril para Inyección Ampoulepack x 5 ml, lote 70243.

Más informaciones por el enlace: https://www.invima.gov.co/medicamentos-y-productos-biologicos-aler-sani/alerta-sanitaria-numero-88-agua-est%C3%A9ril-para-inyecci%C3%B3n-ampoulepack-x-10-ml-lote-70307-y-agua-est%C3%A9ril-para-inyecci%C3%B3n-ampoulepack-x-5-ml-lote-70243-pdf/download.html 

 

 

 
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Varubi (rolapitant) Injectable Emulsion: Health Care Provider Letter – Anaphylaxis and Other Serious Hypersensitivity Reactions

Murilo Freitas - 15:40, 15 de enero de 2018635
Symptoms of anaphylaxis can include wheezing or difficulty breathing; swelling of the face or throat; hives or flushing; itching; abdominal cramping, abdominal pain or vomiting; back pain or chest pain; hypotension or shock.

https://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm592592.htm

 
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