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Carfentanil (also known as Carfentanyl; 4-carbomethoxyfentanyl; R33799) is an analog of the synthetic opioid analgesic Fentanyl. Carfentanil was first synthesized in 1974 by a team of chemists at Janssen Pharmaceutica which included Paul Janssen.

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Description of Carfentanil.

Carfentanil , analog of the synthetic opioid analgesic fentanyl. A unit of carfentanil is 100 times as potent as the same amount of fentanyl.

What is carfentanil?

Carfentanyl is an analog of the synthetic opioid analgesic fentanyl.[1] A unit of carfentanil is 100 times as potent as the same amount of fentanyl, 5,000 times as potent as a unit of heroin and 10,000 times as potent as a unit of morphine.

Carfentanil Overdose:

The toxicity of carfentanil in humans and its ready commercial availability has aroused concerns over its potential use as a weapon of mass destruction by rogue nations and terrorist groups
Carfentanil (also known as Carfentanyl; 4-carbomethoxyfentanyl; R33799) is an analog of the synthetic opioid analgesic Fentanyl. Carfentanil was first synthesized in 1974 by a team of chemists at Janssen Pharmaceutica which included Paul Janssen.

carfentanil effects:

The effect of Carfentanil exceeds Fentanyl and Morphine in 100 and 10000 times, respectively. Median analgesic activity of ED50 for Carfentanil with intravenous administration to rats is 0.41 mg / kg, the effect on the human body begins already with 1 mg.
In 2012, a team of researchers at the British chemical and biological defense laboratories at Porton Down found carfentanil and remifentanil in clothing from two British survivors of the 2002 Moscow theater hostage crisis and in the urine from a third survivor. The team concluded that the Russian military used an aerosol mist of carfentanil and remifentanil to subdue Chechen hostage-takers.

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Authors of a previous paper in the Annals of Emergency Medicine surmised from the available evidence that the Moscow emergency services had not been informed of the use of the agent, but were instructed to bring opioid antagonists.

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