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Washington, D.C., USA- January 13, 2020: FDA Sign at its headquarters in Washington DC. The Food and Drug Administration (FDA or USFDA) is a federal agency of the USA.

Qdolo FDA Approved

Qdolo ™ (tramadol – Athena Bioscience) oral solution, 5mg/mL was approved on Sept. 1, 2020, by the U.S. Food and Drug Administration (FDA). A C-IV controlled substance, it is indicated for treating adults who have severe pain that requires an opioid, but that does not respond to other treatments....
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myMatrixx Names David Dubrof as Chief Sales Officer

myMatrixx, an Express Scripts Company today announced that David Dubrof has been named Chief Sales Officer for the organization. “We’re absolutely thrilled to have David join our team,” said Mike Cirillo, President of myMatrixx. “His 25-plus years of executive management experience in sales,...
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Coronavirus prevention medical surgical masks and hand sanitizer gel for hand hygiene corona virus protection.

MedWatch Update on Hand Sanitizers

During June and July, the FDA has issued a series of warnings that some commercial hand sanitizers contain methanol and it has asked a number of manufacturers to recall their products. Also known as wood alcohol, methanol is intended for industrial use in products such as pesticides and solvents....
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MedWatch Update on Naloxone

In a Safety Communication on July 23, 2020, the FDA alerted prescribers, pharmacies and patients of a new requirement for opioid drugs. It is directing drug companies that make opioids for pain relief and for use in treating opioid use disorder to add information on the labels about the use of naloxone....
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Doctor holding Dexamethasone steroid drug

Update on Dexamethasone Use for COVID-19 Treatment

Preliminary results from a randomized, controlled, open-label, adaptive study on the use of dexamethasone were added to myMatrixx’s “Coronavirus Disease 2019 (COVID-19) – The Search for a Treatment” document. The recovery trial compared a ten day course of dexamethasone 6mg once per day versus...
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