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Opiate warnings and info SWIM did not know
and thanks SWIY for filling me in. first, SWIM thought Fentanyl was the strongest of all; well yes it is for humans, and PLEASE be careful with it. SWIM thanks GOD that the bioavailibility of orally ingested patches is only 1.5%. yes-no matter what quantity is taken orally thru misuse of any patch, your body will ONLY use 1.5% of what is taken. Otherwise SWIM thinks there would be more deaths. Here is the info on the top two OPES, only for animal use. We're talking 5 MILLIGRAMS takes down a full-grown rhino that weighs many tons! How's that for potency! Very long post, copied/pasted from internet searches. Now SWIM knows why people break into Vet's offices. SWIM would leave these 2 alone, and is providing information ONLY for informations sake! So SWIY can stay clear! If SWIY has had any experience with either, SWIM would enjoy hearing any stories. TY
Carfentanil or Carfentanyl is an analogue of the popular synthetic opioid analgesic fentanyl, and is one of the most potent opioids known (also the most potent opioid used commercially). It has a quantitative potency approximately 10,000 times that of morphine and 100 times that of fentanyl, activity in humans starting at about 1 μg. It is marketed under the trade name Wildnil as a tranquilizer for large animals. Carfentanil is intended for animal use only as its extreme potency makes it inappropriate for use in humans. It is thought that in the 2002 Moscow theater hostage crisis, the Russian military made use of an aerosol form of carfentanil to subdue Chechen hostage takers.[1] Its short action, easy reversability and therapeutic index (10600 vs. 300 for fentanyl) would make it a near-perfect agent for this purpose. Wax et al. surmise from the available evidence that the Moscow emergency services had not been informed of the use of the agent, and therefore did not have adequate supplies of naloxone or naltrexone (opioid antagonists) to prevent complications in many of the victims. Assuming that carfentanil was the only active constituent (which has not been verified by the Russian military), the primary acute toxic effect to the theatre victims would have been opioid-induced apnea; in this case mechanical ventilation and/or treatment with opioid antagonists would have been life-saving for many or all victims. and: Technical Information M99 (Etorphine) M99 (etorphine hydrochloride) was synthesised by Bentley & Hardy (1963) and is chemically related to morphine. When given subcutaneously, M99 is 1,000 to 80,000 times more potent than morphine as an analgesic. Its use for immobilising game animals results largely from its ability to cause catatonia at very low dose levels (for example, the total dose for a rhino may be as low as 5 mg). Because of the great risk involved to man and animal in handling this substance, the possession and use of M99 is strictly controlled by law in almost all countries. Novartis enforces this and ensures that M99 and M5050 is only supplied to registered veterinarians. The approved generic name of this compound is etorphine hydrochloride, and the chemical name is 6,14-endoetheno – 7 a (1-(R)-hydroxy-1 methylbutyl)-tetrahydro-nororipavine hydrochloride. M99 is chemically related to morphine. This compound was synthesised by Bentley & Hardy (1963). The acute pharmacology was described in detail by Blane, Bora, Fitzgerald and Lister (1967). In laboratory animals M99 resembles morphine by causing analgesia, catatonia, blockade of conditional reflexes, and anti-diuretic effect. It also resembles morphine by causing excitement in mice, cats and bradycardia and hypotension in rats, dogs, cats and monkeys. When given subcutaneously M99 is 1,000 - 80,000 times more potent than morphine as an analgesic, depending on the test situation. Its use for immobilising game animals results largely from its ability to cause catatonia at very low dose levels. M5050 The approved generic name for this compound is diprenorphine, and the chemical name is N-cyclopropylmethyl-6, 14-endoetheno-7-(1-hydroxy-1-methylethyl)tetrahydro-nororipavine. It is a potent morphine antagonist with an action similar to nalorphine. Its potency, however, was stated by Bentley et al. (1965) to be up to 35 times greater than nalorphine and to have a duration of action two to three times as long. In game animals it produced a rapid and complete reversal of the immobilisation produced by M99. Although it appears that there may be some degree of species variation in the response in practice it has been found that a dosage ratio M5050 to M99 of 1:1 is perfectly satisfactory i.e. 1.3mg diprenorphine produces reversal of the immobilising action of 1mg etorphine. Safety Precautions
M99 is a very potent neuroleptanalgesic which is highly toxic in man. It causes dizziness, nausea and pinpoint pupils, followed by respiratory depression, lowered blood pressure, cyanosis and, in extreme cases, loss of consciousness and cardiac arrest. If there is any danger that M99 may have been injected or absorbed, the following steps should be taken IMMEDIATELY!!!!! In case of:
Reversing Agents Inject 2-3mls Narcan (0.4mg/ml naloxone) preferably intravenously or alternatively intramuscularly, and repeat at intervals of 2 to 3 minutes until symptoms are reversed. In the event of Narcan being unavailable, or in a situation of extreme emergency, the following information is provided for possible guidance: Inject 0.1ml M5050 preferably intravenously or alternatively intramuscularly, but if the actual quantity of M99 injected or absorbed is known inject an equal quantity of M5050. If respiratory depression is not reversed, repeat the dose after 2 or 3 minutes. Recurrence of morphine-like effects may occur due to enterohepatic recycling. (M5050 may also induce a hallucinatory state). IT IS VITAL THAT ADEQUATE RESPIRATION AND HEARTBEAT BE MAINTAINED, IF NECESSARY BY MEANS OF ARTIFICAL RESPIRATION AND EXTERNAL HEART MASSAGE, UNTIL MEDICAL HELP ARRIVES. Adequate respiration must be maintained by: (a) Ensuring that the airway is clear by placing the patient in the recovery position removing dentures or any other oral obstruction, andMedical Assistance Once the emergency measures have been undertaken as set out above, expert medical attention should be summoned immediately. Pending the transfer of the patient to medical care the supportive treatment to maintain the respiration and heartbeat should be continued as required. Respiratory arrest beyond 4 minutes may cause irreversible brain damage. Emergency Pack This must be carried by all users. It should contain explicit instructions as well as:
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