EDIC of National Institute for Diabetes & Endocrinology

  • Home
  • Egypt
  • Cairo
  • EDIC of National Institute for Diabetes & Endocrinology

EDIC of National Institute for Diabetes & Endocrinology A service unit committed to provide unbiased drug information to health care professionals, patients &/or consumers.

03/07/2017

Clinical pharmacy (workshop)

05/03/2017
30/06/2016

The US Food and Drug Administration today approved a new insulin inhaler for use in treating diabetes, its first in years. The product, which is made by California-based MannKind Corporation, uses...

The use of this drug has been increasing due to its value as a last resort treatment for multi-drug resistant organisms....
06/04/2016

The use of this drug has been increasing due to its value as a last resort treatment for multi-drug resistant organisms.
http://www.drugs.com/monograph/colistimethate-sodium.html

Colistimethate Sodium reference guide for safe and effective use from the American Society of Health-System Pharmacists (AHFS DI).

15/01/2016

Annu Rev Neurosci. 2007;30:259-88. Research Support, Non-U.S. Gov't; Review

24/12/2015

Tienam Thrombocytopenia Side Effect Reports
This Thrombocytopenia side effect was reported by a health professional from FR. A 12-year-old patient (weight:NA) experienced the following symptoms/conditions: NA. The patient was prescribed Tienam 500mg/500mg, Poudre Pour Perfusion (dosage: Unk), which was started on May 24, 2013. Concurrently used drugs: •Vancomycin (Unk)
•Zovirax (Unk)
•Cancidas (Unk)
•Fortum (Unk)
•Methotrexate (Unk)
•Cytarabine (Unk)
•Methylprednisolone (Unk)
•Nelarabine (Unk)
When starting to take Tienam 500mg/500mg, Poudre Pour Perfusion the consumer reported the following symptoms: •Agranulocytosis
•Leukopenia
•Thrombocytopenia
The patient was hospitalized. These side effects may potentially be related to Tienam 500mg/500mg, Poudre Pour Perfusion.

19/12/2015

SGLT2 Inhibitor Diabetes Drugs May Cause Ketoacidosis: FDA
he US Food and Drug Administration (FDA) warned today that sodium-glucose cotransporter-2 (SGLT2) inhibitors used to treat type 2 diabetes may lead to ketoacidosis requiring hospitalization.

The warning includes the SGLT2 inhibitors canagliflozin (Invokana, Johnson & Johnson), dapagliflozin (Farxiga, AstraZeneca), and empagliflozin (Jardiance, Lilly/Boehringer), as well as three combination products that include an SGLT2 inhibitor: canagliflozin plus metformin (Invokamet, Johnson & Johnson), dapagliflozin plus metformin extended release (Xigduo XR, AstraZeneca), and empagliflozin plus linagliptin (Glyxambi, Lilly/Boehringer).

A search of the FDA Adverse Event Reporting System database identified 20 cases of acidosis reported as diabetic ketoacidosis (DKA), ketoacidosis, or ketosis in patients treated with SGLT2 inhibitors from March 2013 to June 6, 2014, the FDA said.
http://www.medscape.com/viewarticle/844754

A service unit committed to provide unbiased drug information to health care professionals, patients &/or consumers.

04/08/2015

Q: Of the following which can be used as treatment of calcium channel blockers toxicity?
A) Intravenous calcium
B) Atropine
C) Hyperinsulinemia-euglycemia therapy
D) lipid emulsion therapy
E) All of the above
Answer: E
Mild toxicity of Calcium channel blockers usually resolved with supportive treatment with IVF and transient support with pressors. In case of acute overdose, activated charcoal, gastric lavage, and polyethylene glycol may be used to decontaminate the gut.
In case of severe toxicity, Intravenous calcium can be used. Atropine as well as temporary intravenous pacemaker may be required for un-resolving bradycardia/blocks.
Hyperinsulinemia-euglycemia therapy has been advocated for treatment. Increased insulin mobilizes glucose from peripheral tissues to serve as an alternative fuel source for the heart. Treatment with lipid emulsion therapy has been described too with same mechanism of action.
منقول

http://www.fda.gov/Drugs/DrugSafety/ucm439484.htm
02/08/2015

http://www.fda.gov/Drugs/DrugSafety/ucm439484.htm

[03-24-2015] The U.S. Food and Drug Administration (FDA) is warning that serious slowing of the heart rate can occur when the antiarrhythmic drug amiodarone is taken together with either the hepatitis C drug Harvoni (ledipasvir/sofosbuvir) or with Sovaldi (sofosbuvir) in combination with another dir…

Address

Cairo

Telephone

+20223643233

Website

Alerts

Be the first to know and let us send you an email when EDIC of National Institute for Diabetes & Endocrinology posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Practice

Send a message to EDIC of National Institute for Diabetes & Endocrinology:

Share

Share on Facebook Share on Twitter Share on LinkedIn
Share on Pinterest Share on Reddit Share via Email
Share on WhatsApp Share on Instagram Share on Telegram