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2004 Guide to Psychiatric Drug Interactions
2004 Guide to Psychiatric Drug Interactions

... health professionals who practice in the pharmaceutical industry. This is because the number of prescription medicines that were initially approved by the FDA as safe and effective but which then had to be removed from the market due to unacceptable DDIs, including terfenadine, cisapride, astemizole ...
Bulletin #94
Bulletin #94

... Effective April 1, 2003 the EDS criteria for the following products will be as indicated: raloxifene HCl, tablet, 60mg (Evista-LIL) Exception Drug Status criteria was revised to read as follows: (a) For treatment of osteoporosis in patients who do not respond to etidronate disodium/calcium (Didrocal ...
Paul G. King Consulting
Paul G. King Consulting

... impurity profile and physical-state structure as before the change, no matter how minor the change. [After all, based on the published evidence, the critical impurity in the l-tryptophan case only became a consumer safety problem after the purification process was changed to use less activated charc ...
Slide 1
Slide 1

... 3) Not suitable for bitter and irritating drugs 4) Less patient compliance 5) No eating, Drinking and smoking is allowed 6) Highly ionic drugs can not be administered ...
Pharmacologyonline 1: 613-624 (2011) Thanigavelan et al.
Pharmacologyonline 1: 613-624 (2011) Thanigavelan et al.

... size and numbers of villai. 4. The process of Pudam should be done in a closed environment with adequate air flow. 5. In most of the Pudam process, cow dung cakes have to be used for burning. But for some preparation of Parpams, barks, goat dung cakes are used, especially when high temperature is ne ...
Development and in-vitro characterization of sustained release
Development and in-vitro characterization of sustained release

... consumed by patients suffering from acute and chronic pains. However these drugs are not consumed by patients as per prescription advice. Patients very often miss a dose and compliance to dosage regimen always remains a question mark. To overcome these kinds of issues and also to maintain a continuo ...
USP Overview and Some Current Activities
USP Overview and Some Current Activities

... on the Specification Limits for Residues of Metal Catalysts (CPMP/SWP/4446/00) lists 14 catalysts used in pharmaceutical synthesis – Exclude zinc and iron, which are not toxic at levels relevant in pharmaceuticals ...
PHYSICOCHEMICAL CHARACTERIZATION AND IN-VITRO DISSOLUTION BEHAVIOR OF GLICLAZIDE –SOLUPLUS SOLID DISPERSIONS
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... crystal habits, complexation, using surfactants and co-solvents, solid dispersions, etc have been extensively studied. Chemical modifications such as prodrugs, salt formation, and polar group incorporation were also studied. Solid dispersion is an attractive approach to improve solubility of hydroph ...
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Overdose Prevention with Community Based Naloxone: An …
Overdose Prevention with Community Based Naloxone: An …

... 9. concurrent SSRI or TCA anti-depressant prescription 10. Prisoner released from custody 11. Release from opioid detoxification or mandatory abstinence program 12. Voluntary request from patient 13. Patients in methadone or buprenorphine detox/maintenance (for addiction or pain) 14. Patient may hav ...
training workshop on pharmaceutical quality, good manufacturing
training workshop on pharmaceutical quality, good manufacturing

... – Generally required for solid oral dosage forms • Critical use • Narrow therapeutic range • Bioavailability problems associated with the active ingredient • Problematic polymorphism, excipient interaction, or sensitivity to manufacturing processes ...
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... Recently for local treatment of variety of colonic diseases and also for those drugs where a delay in drug absorption is required from a therapeutic point of view as in case of nocturnal asthma, arthritis and cardiac arrhythmias that are affected by circadian biorhythms 17. Apparently the colon has ...
Orally Disintegrating Tablets
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... Such a technology evolution has been evident for orally disintegrating tablets (ODTs). Designed to disintegrate rapidly on contact with saliva and enable oral administration without water or chewing, these formulations offer increased convenience and ease of administration with the potential to impr ...
Severe hepatotoxicity by Indian Ayurvedic herbal products: A
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... The term drug refers basically to any synthetic drug, herbal drug, and dietary supplement including the herbal one. For differentiation of the hepatocellular, cholestatic or mixed form of hepatotoxicity caused by drugs and dietary supplements (DDS), serum activities of alanine aminotransferase (ALT) ...
Computational Biology
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... sequence, such as imatinib binding to LCK but not SRC. ABL and the imatinib-resistant ABL mutants are of particular structural interest because some compounds bind with good affinity to all forms (e.g., ZD-6474), whereas BIRB-796 has a strong preference for a particular mutant. Key insights should r ...
Prescribing of COX-2 inhibitors in Germany after safety warnings
Prescribing of COX-2 inhibitors in Germany after safety warnings

... new, innovative and more expensive drugs were calculated. Finally, prescribing of relevant drug classes by different medical specialist groups was analysed in order to assess the potential for pharmaceutical interventions. Thus, pharmacists may improve patient safety when different prescribers are n ...
GLAUCOMA MEDICATIONS - Nevada Optometric Association
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... • Safer and less invasive than the intravitreal route • Systemic absorption is low • Lower systemic side effects while providing a localized drug effect • Substantial evidence indicating that drugs administered subconjunctivally can reach the vitreous effectively • Injectable microspheres have alrea ...
Drug Repositioning Approaches for the Discovery of New ’s Disease REVIEW
Drug Repositioning Approaches for the Discovery of New ’s Disease REVIEW

... solution to overcome some of these impending pharmaceutical industry and medical challenges [8–10]. “Drug repositioning”, also referred to as “drug repurposing”, is the process of identifying new indications for existing drugs (Fig. 1). In addition to approved drugs, this approach can also salvage d ...
6 Solutions Copyright Pharmaceutical Press www.pharmpress.com
6 Solutions Copyright Pharmaceutical Press www.pharmpress.com

... dosage forms is that they are always much larger and more bulky than their comparable solid formulation. This makes them heavier and more difficult to transport. Coupled with this is the fact that, traditionally, pharmaceutical liquids are packed in glass bottles. These are obviously prone to breaka ...
See Important Disclosures and Disclaimers at the end of this report
See Important Disclosures and Disclaimers at the end of this report

... include efficacy when used as a single agent, less toxicity in terms of reported adverse events, less bone marrow toxicity, and a lack of severe side effects, which may enable the drug to be combined with other cytotoxic agents. Evomela® (melphalan for injection) Spectrum launched its sixth drug, Ev ...
1 - European Commission
1 - European Commission

... is to specify the administrative procedures in terms of issuing permits and permissions defined under the Act, as well as to regulate under the Act the fees for issuing these. The provisions on limiting the dispensing of OTC medicinal products (Article 71a of the Pharmaceutical Act of 6 September 20 ...
IN-VITRO EVALUTION OF COMMERCIALLY AVAILABLE SUSTAINED RELEASE CAPSULE CONTAINING DILTIAZEM HYDROCHLORIDE
IN-VITRO EVALUTION OF COMMERCIALLY AVAILABLE SUSTAINED RELEASE CAPSULE CONTAINING DILTIAZEM HYDROCHLORIDE

... exponent, n was greater than 0.85 (Table 4). For the system exhibiting super case II transport, the dominant mechanism for drug transport was polymer relaxation as the gel swells. CONCLUSION ...
Final BMEIdea Project Submission
Final BMEIdea Project Submission

... The barcode approach was considered for IVIS drug recognition. However, personal consultation with clinicians has revealed that active drug recognition, such as scanning a barcode before injection, introduces another step to the IV injection procedure that is not clinically realistic. Additionally, ...
Impurities: Residual Solvents ICH: Q3C
Impurities: Residual Solvents ICH: Q3C

... -does not address all possible solvents, only those identified in drugs at that time -does not address solvents deliberately used as excipients nor solvates. ...
EXTENDED RELEASE ROPINIROLE TABLET FORMULATION PREPARED BY MELT GRANULATION TECHNIQUE  Research Article
EXTENDED RELEASE ROPINIROLE TABLET FORMULATION PREPARED BY MELT GRANULATION TECHNIQUE Research Article

... The present work was aimed to develop an extended release matrix tablet formulation of Ropinirole hydrochloride (ROH) using polymers like polyox WSR 301, carbopol 71G, kollicoat SR 30 D and waxes like cetyl alcohol (CA), carnauba wax (CW), glyceryl monostearate (GMS). Wet granulation, direct compres ...
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Compounding

Pharmaceutical compounding (done in compounding pharmacies) is the creation of a particular pharmaceutical product to fit the unique need of a patient. To do this, compounding pharmacists combine or process appropriate ingredients using various tools. This may be done for medically necessary reasons, such as to change the form of the medication from a solid pill to a liquid, to avoid a non-essential ingredient that the patient is allergic to, or to obtain the exact dose(s) needed or deemed best of particular active pharmaceutical ingredient(s). It may also be done for more optional reasons, such as adding flavors to a medication or otherwise altering taste or texture. Compounding is most routine in the case of intravenous/parenteral medication, typically by hospital pharmacists, but is also offered by privately owned compounding pharmacies and certain retail pharmacies for various forms of medication. Whether routine or rare, intravenous or oral, etc., when a given drug product is made or modified to have characteristics that are specifically prescribed for an individual patient, it is known as ""traditional"" compounding.Due to the rising cost of compounding and the shortage of drugs, many hospitals have shown a tendency to rely more upon large-scale compounding pharmacies to meet their regular requirement, particularly of sterile-injectable medications. When compounding is done on bulk production of a given formulation rather than patient-specific production, it is known as ""non-traditional"" compounding (which, as discussed below, is arguably not ""compounding"" but rather ""manufacturing""). This development raises concerns about patient safety and makes a case for proper regulatory control and monitoring.
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