Cytotoxic drugs definition

Cytotoxic drugs means any drug defined by the department as extremely hazardous
Cytotoxic drugs means, for purposes of this chapter, any drug defined by the
Cytotoxic drugs means drugs that work by targeting and damaging cells that grow at a rapid rate.

Examples of Cytotoxic drugs in a sentence

  • Choi and Jeon (2021) clarify that a key factor be- yond new theories of bundling in two-sided markets is that a platform’s ability to cope with aggressive competition is limited by the non-negative price constraint.

  • Cytotoxic drugs should only be handled by staff specially trained in the safe handling of such preparations.

  • Cytotoxic drugs interfere with cell division, but as this action is not specific to tumour cells, normal cells may also be damaged.

  • Cytotoxic drugs should be administered in a dedicated therapeutic environment with appropriate facilities for safe administration and within safe working staffing levels.

  • Cytotoxic drugs must be easily identifiable by all personnel involved in their handling.

  • The product should be immediately returned to pharmacy, or disposed of according to the Trust Disposal of Waste procedure. Any cytotoxic drugs received on the ward or day units, but not administered, must be safely returned to the Pharmacy Department as soon as possible and the pharmacy staff informed of the reason why it was not administered. Cytotoxic drugs that are to be transported outside of the hospital should be placed in sturdy, leak- proof transport bags or boxes.

  • Cytotoxic drugs must be transported so as to provide adequate physical and chemical protection for the drug and the drug handler.

  • Cytotoxic drugs and the aquatic environment: estimation of bleomycin in river and water samples.

  • Cytotoxic drugs should NOT be given if there is any doubt regarding the patency of the venous access device.

  • All such storage areas will be clearly labelled with cytotoxic warnings. Main stocks of cytotoxic drugs will be held in the Pharmacy Department, under appropriate conditions. Clinical trial supplies of cytotoxic drugs should be kept separate from main stocks in pharmacy. Cytotoxic drugs should not routinely be available as ward stock.

Related to Cytotoxic drugs

  • Biological agent shall mean any pathogenic (disease producing) micro-organism(s) and/or biologically produced toxin(s) (including genetically modified organisms and chemically synthesized toxins) which cause illness and/or death in humans, animals or plants.

  • Toxic chemical means a chemical or chemical category listed in 40 CFR 372.65.

  • Biological Samples means any physical samples obtained from Study Participants in accordance with the Protocol for the purposes of the Study.

  • Dangerous drug means any of the following:

  • Narcotic drug means any of the following, whether produced directly or indirectly by extraction from substances of vegetable origin, or independently by means of chemical synthesis, or by a combination of extraction and chemical synthesis:

  • Antibody means a molecule or a gene encoding such a molecule comprising or containing one or more immunoglobulin variable domains or parts of such domains or any existing or future fragments, variants, modifications, or derivatives thereof, but excluding single variable domains (heavy or light) of such antibodies.

  • Drug addiction means a disease characterized by a

  • cosmetic product means any substance or mixture intended to be placed in contact with the external parts of the human body (epi­ dermis, hair system, nails, lips and external genital organs) or with the teeth and the mucous membranes of the oral cavity with a view exclusively or mainly to cleaning them, perfuming them, changing their appearance, protecting them, keeping them in good condition or correcting body odours;

  • Vaccine means a specially prepared antigen which, upon administration to a person, will result in immunity and, specifically for the purposes of this rule, shall mean influenza and pneumococcal vaccines.

  • Prescription drugs means drugs, medicine and controlled substances which by law can only be prescribed for human use by persons authorized by law.

  • Therapeutic diet means meals served that are soft, low-fat, low-sodium or controlled calorie.

  • Cannabinoid edible means food or potable liquid into which a cannabinoid concentrate, cannabinoid extract or dried marijuana leaves or flowers have been incorporated.

  • Substances means chemical elements and their compounds in the natural state or obtained by any production process, including any additive necessary to preserve the stability of the products and any impurity deriving from the process used, but excluding any solvent which may be separated without affecting the stability of the substance or changing its composition;

  • Methamphetamine means methamphetamine, any salt, isomer, or salt of an isomer of methamphetamine, or any compound, mixture, preparation, or substance containing methamphetamine or any salt, isomer, or salt of an isomer of methamphetamine.

  • Cancer drug means a prescription drug used to treat:

  • toxic waste or "toxic substance" under any provision of Environmental Law and shall also include, without limitation, petroleum, petroleum products, asbestos, polychlorinated biphenyls and radioactive materials;

  • Chemical dependency means the physiological and psychological addiction to a controlled drug or substance, or to alcohol. Dependence upon tobacco, nicotine, caffeine or eating disorders are not included in this definition.

  • Weapons means an instrument or device of any kind that is used or designed to be used to inflict harm including, but not limited to, rifles, handguns, shotguns, antique fire- arms, knives, swords, bows and arrows, BB guns, pellet guns, air rifles, electronic or other stun devices, or fighting imple- ments.

  • Radionuclide means a radioactive element or a radioactive isotope.

  • Nonprescription drugs means nonnarcotic medicines or drugs which may be sold without a prescription and are prepackaged and labeled for use by the consumer in accordance with the requirements of the statutes and regulations of this state and the federal government;

  • Active Pharmaceutical Ingredient or “API” shall mean one or more of the following active pharmaceutical ingredients: tenofovir alafenamide (“TAF”), tenofovir disoproxil fumarate (“TDF”), elvitegravir (“EVG”), and cobicistat (“COBI”).

  • Drugs means (a) substances recognized in the official United

  • Counterfeit drug means a drug that, or the container or

  • Receptor means enclosed spaces, conduits, protected groundwater sources, drinking and non-drinking water wells, surface water bodies, and public water systems which when impacted by chemicals of concern may result in exposure to humans and aquatic life, explosive conditions or other adverse effects on health, safety and the environment as specified in these rules.

  • toxic substances as defined by the Toxic Substances Control Act, as amended from time to time (“TSCA”), (4) “hazardous materials” as defined by the Hazardous Materials Transportation Act, as amended from time to time (“HMTA”), (5) asbestos, oil or other petroleum products, radioactive materials, urea formaldehyde foam insulation, radon gas and transformers or other equipment that contains dielectric fluid containing polychlorinated biphenyls and (6) any substance whose presence is detrimental or hazardous to health or the environment, including, without limitation, microbial or fungal matter or mold, or is otherwise regulated by federal, state and local environmental laws (including, without limitation, RCRA, CERCLA, TSCA, HMTA), rules, regulations and orders, regulating, relating to or imposing liability or standards of conduct concerning any Hazardous Materials or environmental, health or safety compliance (collectively, “Environmental Requirements”). As used in this Contract: “Release” means spilling, leaking, pumping, pouring, emitting, emptying, discharging, injecting, escaping, leaching, dumping or disposing.

  • Pesticide means any substance or mixture of substances intended for preventing, destroying, repelling, or mitigating any pest, or intended for use as a plant regulator, defoliant, or desiccant, other than any article that: