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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Is paracetamol being prescribed and used at the correct therapeutic dose in the children population in South Africa?

Patel, Aadila January 2014 (has links)
>Magister Scientiae - MSc / When used at the recommended and approved therapeutic dose, paracetamol is effective. Paracetamol is available in various forms and easily accessible from general dealers and pharmacies. The liquid form is the preferred form given with a device to children. Paracetamol is effective within a defined therapeutic range; however, are prescribers and caregivers using paracetamol as authorised by regulators? A qualitative review of product specific labelling and the department of health recommendations was conducted and evaluated by means of arithmetic means differences to the regulator requirements. Surveys of healthcare professionals and caregivers determined the quantity administered and to establish if a device was used. The dosing information from product specific labelling, the department of health and the regulator source were reviewed for recommended dose, frequency of administration, maximum daily dose and recommendations for overdose treatment. There are similarities and differences with the null hypothesis being proven. Product labelling and department of health recommendations do not conform to the regulator accepted therapeutic dose. There was no unambiguous legislative medicine guideline on the age of a child with children between six and twelve being underdosed with liquid paracetamol in terms of volume and strength.
2

Investigations into the use of continuous low-level medication for the control of helminths in the ruminant

Dobbins, Sally Elizabeth January 1984 (has links)
The work presented in this thesis is concerned with the chemotherapy of parasite infestations in the ruminant with the anthelmintic thiophanate [diethyl 4,4'-o-phenylene bis (3-thioallophanate)]. A new concept of administration was investigated, namely continuous low-level anthelmintic medication. Two aspects were studied which divide conveniently into two sections. In Section 1, following preliminary trials undertaken to assess the low-level anthelmintic activity of thiophanate, the effects are assessed when this drug is administered continually directly into the rumen of parasitised sheep. Thiophanate was infused at dosages between 3.0 and 5.0 mg per kg bodyweight over various periods of medication against various developmental stages of gastro-intestinal parasites. The daily drug release rate. required to inhibit egg hatch and eliminate the worm burden is established. A minimum daily release rate of 3.0 mg per kg bodyweight was shown to be required to completely inhibit egg hatch and 4.5 mg per kg for effective vermicidal activity. In similar experiments, the anthelmintic activities of levamisole (s-(-)-2,3,5,6-tetrahydro-6-phenylimidazo (2,1-b) thiazole), febantel (N-(2-(2,3-bis-(methoxycarbonyl)-guanidino)-5-(phenyl-thio)-phenyl)-2-methoxy-acetamide) and briefly oxfendazole (5-(phenylsulfinyl)-IH-benzimidazol-2yl) carbamate) were also examined. In Section 2, the development of an intra-ruminal bolus incorporating thiophanate and designed to release drug at a predetermined rate over an extended period of time is described. Experiments were carried out in sheep to assess the bolus density required for retention within the reticulo-rumen (monitored by direct bolus recovery), to compare various density factors (iron powder, iron bar core, iron shot and sand) and to assess the average drug release rate from different matrix formulations (based on fatty acids, palmitic acid and paraffin wax) when the boluses were dosed singly or in pairs. The development of a stable "carrier" on which to load a suitable matrix is also described, the majority of the experiments undertaken utilising this "carrier". The effect on the drug release rate of incorporating various "leaching aids" (digestible materials, wetting and soluble agents) into the matrix is examined and preliminary anthelmintic trials undertaken in experimentally infected lambs. The required drug release is achieved when the boluses are administered in pairs. The anthelmintic activity is confirmed. Possible matrices suitable for use as a single bolus administration were produced. The advantages of this form of anthelmintic medication over the single therapeutic dose are discussed along with some indications for further studies that emerged.

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