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Though CR drugs are commonly used in psychiatry, clinicians appear to have a limited understanding of how they are released for absorption once ingested. Due to lack of awareness of this phenomenon to both patients and the physicians, anxiety has ensued in some patients. Some clinicians have been puzzled or have been dismissive when faced with curious patients wanting to know more after they had observed tablet-like looking structures in faeces. We present two cases from our clinical setting and a few drawn from the World Wide Web to highlight the role of CR medications and their association with the ghost pill phenomenon. The ghost pill phenomenon occurs with certain CR medications. It is inevitable that some patients will see what looks like tablets or capsules in faeces. Awareness among patients and carers would also help to allay anxiety.

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Though CR drugs are commonly used in psychiatry, clinicians appear to have a limited understanding of how they are released for absorption once ingested. Pharma Technol On-Line 25 : 1—

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It induces liver enzymes, which reduces its effectiveness and the effectiveness of other drugs such as phenytoin, oral contraceptives, warfarin and corticosteroids. Adverse effects of carbamezepine are similar to those seen with phenytoin.

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There are many routes of parenteral administration, some of which are intended for a drug to have a systemic effect and others for a local effect. See Figure (In some definitions, parenteral is synonymous with injection (for example in the Medicines Act), but here the term is used to describe all routes of administration that are not enteral. ) The vast majority of drugs are administered by mouth as pills, capsules, tablets or liquids. Following oral administration, absorption of a drug is from the stomach or intestine directly via the hepatic portal system to the liver before reaching the general circulation. The liver is the main site of drug metabolism and inactivation. Many factors affect drug absorption from the gastrointestinal tract, including lipid solubility of the drug; its molecular weight; the pH of the local environment; the surface area of the absorbing membrane; gastric emptying time; the rate of removal from the gastrointestinal tract by the blood and the degree of plasma protein binding of the drug once in the blood stream.


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The only exception to this rule is when a patient must always receive the same brand of a drug because different preparations can result in different blood levels of the drug. No details of dosages are given in this book, because these are subject to change and often have to be varied to suit individual patients.

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