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Clonidine For Opiate Withdrawal Symptoms: Does It Help?

Clonidine is an antihypertensive drug originally synthesized in the early 1960s by chemists employed under the pharmaceutical company Boehringer Ingelheim.  At the time, the chemists intended to develop a peripherally-active adrenergic nasal decongestant to be administered in the form of nose drops.  In the process, the chemists sought to modify amidines to fit the chemical …

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Kratom For Opiate Withdrawal: A Popular “Natural” Intervention

Kratom (Mitragyna speciosa) is a tropical evergreen tree from the coffee family (Rubiaceae) native to Indonesia, Papa New Guinea, Thailand and other parts of Southeast Asia.  The kratom tree produces leaves containing psychoactive compounds, and when ingested, these compounds are capable of eliciting opioidergic and/or stimulatory effects.  Although it is estimated that kratom leaves contain …

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Gabapentin For Opiate Withdrawal

Gabapentin is rumored to have been synthesized by chemists in the 1970s in attempt to develop an antispasmodic agent.  After its synthesis, rights to gabapentin were acquired by Parke-Davis (a subsidiary of Pfizer) whereafter it underwent clinical trials that evaluated its safety and anticonvulsant efficacy in the treatment of seizures.  Clinical trial data indicated that …

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Naltrexone & Weight Loss: What Should You Expect?

Naltrexone is a chemical initially synthesized in 1963 and patented thereafter by the pharmaceutical company Endo Laboratories in 1967.  It is considered a substituted derivative of oxymorphone in that the tertiary amine methyl-constituent is replaced with an allyl group (specifically an N-cyclopropylmethyl group) – or a longer chain of carbon atoms.  It was initially approved …

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Naltrexone Side Effects & Adverse Reactions (List)

Naltrexone is a pure opioid receptor antagonist utilized principally for the treatment of alcohol and opioid dependence.  As an opioid receptor antagonist, naltrexone competitively binds to mu-opioid receptor (MOR) and kappa-opioid receptor (KOR) sites with higher affinity than opioid agonists, thereby attenuating receptor activation.  Should an individual administer an opioid agonist (e.g. morphine) while taking …

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Fioricet “High”: Intoxication From Butalbital-Containing Agents

Fioricet is a medication approved by the FDA for the treatment of three specific types of headaches including: tension, muscle contraction, and post-dural puncture.  It contains a unique blend of a barbiturate (butalbital 50 mg), a pain reliever (acetaminophen 300 mg), and a stimulant (caffeine 40 mg); hence the reason it is sometimes abbreviated as Butal-Acet-Caff.  …

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Impulse Control Disorder (ICD): Causes, Symptoms, Treatment

Impulse control disorder (ICD) is an overarching classificatory label given to psychiatric disorders characterized by inability to resist impulses (or urges) that yield deleterious implications.  Examples of impulse control disorders include: compulsive gambling, incessant sexual encounters, and binge shopping.  If unrecognized and/or unaddressed for an extended duration, an impulse control disorder may ruin a person’s: …

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