The misuse of drugs is a major problem throughout the world. This is, in part, due to the lack of information provided to the patient. The responsibility for this must be shared by the prescribing doctor, manufacturer, the individual dispensing the drug and the consumer himself.
Even in developed countries, over half the patients do not know how, when and with what to take their medicines. The vast majority have no information on potential side-effects. The situation is worse in India.
Many patients complain that not enough information is provided to them. This is especially common in government hospitals and dispensaries where a few doctors cater to a large number of patients and thus have little time during an ordinary consultation. Several surveys have shown that 30-80% of patients fail to comply with the physicians’ instructions on the usage of drugs.
A patient’s knowledge remains insufficient if he is only provided verbal information. It is important to ensure appropriate labelling of the drug package, provide a simple written plan of therapy and leaflets on the drugs prescribed, send reminders, ensure follow up visits and facilitate self-management.
The 8 following is the minimum information to be provided on the leaflets given to the patient:
This warmly commended paper considers the debate over the ethics of death assisted by a physician, keeping personal and professional integrity in focus. The moral dilemma consequent to conflicting directives of conscience is addressed. ‘Considerable reflection, deliberation, consultation and study may be required to arrive at a position which is considered reasonable.’
Whilst killing a patient can be looked at as the ultimate harm, deaths that bring a full life to a peaceful close has long been regarded as merciful. The description of pneumonia as ‘the old man’s friend’ is an example. The foregoing of life-sustaining intervention to allow the patient to die is another.
It is the active induction of death, conflicting, as it does, with the duty to preserve life, that has made debate necessary. Kass put up an interesting argument. An event can be beneficial only to one who continues to gain from it. The authors counter by pointing out that an act removing an evil (in this case unrelievable suffering) can also be termed beneficial. .
Participation by a physician in capital punishment is contrasted with voluntarily assisting a terminally ill person in agony to die.
The journal also features six other papers (pages 17-19, 19-23, 24-25, 28-35, 36-43, 44-45) on this theme. The last two papers feature death in hospice, Dame Cicely Saunders bringing the discussion to a close. A table on page 39 features ‘The death with dignity act’.
A twenty-four page supplement considers such issues as priorities in genetic medicine, informed consent in prenatal testing, legal aspects, commercial aspects of genetic diagnostics, the use of human growth hormone and the policy for screening to uncover cystic fibrosis.