OMICS International

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Scheduled Drugs


As per available reports about10 relevant journals, 71 Conferences, 6 workshops are presently dedicated exclusively to scheduled drugs and about 1543 articles are being published on scheduled drugs.

Drug  substances and sure chemicals accustomed build medication area unit classified into 5 (5) distinct classes or schedules relying upon the drug’s acceptable medical use and also the drug’s abuse or dependency potential. The abuse rate may be a determinate think about the programming of the drug; for instance, Schedule I medication area unit thought of the foremost dangerous category of medicine with a high potential for abuse and probably severe psychological and/or physical dependence because the schedule drug changes-- Schedule II, Schedule III, etc., thus will the abuse potential-- Schedule V medication represents the smallest amount potential for abuse. a list of medicine and their schedule area unit set at drug Act (CSA) programming or CSA programming by Alphabetical Order. These lists describes the essential or parent chemical and don't essentially describe the salts, isomers and salts of isomers, esters, ethers and derivatives which can even be classified as controlled substances. These lists area unit supposed as general references and aren't comprehensive listings of all controlled substances.

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Scope and Importance

Schedule I medication, substances, or chemicals area unit outlined as medication with no presently accepted medical use and a high potential for abuse. Schedule I medication area unit the foremost dangerous medication of all the drug schedules with probably severe psychological or physical dependence. Some samples of Schedule I medication are: hard drug, acid diethylamide (LSD), marijuana (cannabis), 3,4-methylenedioxymethamphetamine (ecstasy), Quaalude, and peyote.
Schedule II medication, substances, or chemicals area unit outlined as medication with a high potential for abuse, less abuse potential than Schedule I medication, with use probably resulting in severe psychological or physical dependence. These medication also are thought of dangerous. Some samples of Schedule II medication are: cocain, ice, methadone, anodyne (Dilaudid), meperidine hydrochloride (Demerol), oxycodone (OxyContin), fentanyl, Dexedrine, Adderall, and Ritalin.
Schedule III medication, substances, or chemicals area unit outlined as medication with a moderate to low potential for physical and psychological dependence. Schedule III medication abuse potential is a smaller amount than Schedule I and Schedule II medication however over Schedule IV. Some samples of Schedule III medication are: Combination product with but fifteen milligrams of hydrocodone per dose unit (Vicodin), product containing but ninety milligrams of antitussive per dose unit (Tylenol with codeine), ketamine, anabolic steroids, androgenic hormone.
Schedule IV medication, substances, or chemicals area unit outlined as medication with a coffee potential forabuse and low risk of dependence. Some samples of Schedule IV medication are: benzodiazepine, Soma, Darvon, Darvocet, Valium, Ativan, Talwin, Ambien
Schedule V medication, substances, or chemicals area unit outlined as medication with lower potential for abuse than Schedule IV and incorporates preparations containing restricted quantities of sure narcotics. Schedule V medication area unit typically used for medicine, medicament, and analgesic functions. Some samples of Schedule V medication are: Cough preparations with but two hundred milligrams of antitussive or per a hundred milliliters (Robitussin AC), Lomotil, Motofen, Lyrica, Parepectolin.


Market Analysis

The market was valued at US$1.56 billion in 2013 and is estimated to reach a value of US$4.49 billion by the end of 2020.With the help of regulatory affairs outsourcing, life science, pharmaceutical, and medical device manufacturing companies are able to get their drugs or devices approved or launched in the global market. Regulatory affairs outsourcing by biopharmaceutical companies has minimized losses due to recalls and product approval delays. Regulatory affairs service providers also provide effective services such as clinical trial services, medical writing, and pharmacovigilance to biotech, pharma, and medical device companies.
 

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This page was last updated on 14th Sep, 2015

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