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Latest Drugs
Nutrition and Dietetics Drug Data - A-Z (English)
Drug Class Description
Fat supplements (Foods (ACBS approved)).Generic Name
EmulsionDrug Description
Calogen is a Food for Special Medical Purposes for use under medical supervision. Calogen is a high energy, long chain triglyceride fat emulsion. Calogen can be used to supplement or fortify the diet of patients who are unable to meet their energy requirements from normal food and drink. Calogen is suitable for patients requiring electrolyte restrictions, can be used to replace milk in protein restricted diets, and can be used as an energy enhancer in tube and sip feeds.Presentation
Calogen is available in 200ml and 500ml plastic bottles, in 3 flavours: Neutral, Banana, Strawberry.Indications
For enteral use only. ACBS approved, prescribable on Form FP10 (GP10 in Scotland) for the following indications: Disease related malnutrition; malabsorption states, or other conditions requiring f o rtification with a high fat supplement with or without fluid restriction.Adult Dosage
Shake well before opening. Dosage determined by a clinician or dietitian and is dependent on the age, bodyweight, and medical condition of the patient. The recommended dose is 3 x 30ml per day, unless specified by a clinician or dietitian. Can be taken undiluted or diluted with milk, water, or mixed into foods.
Child Dosage
Neutral Calogen is suitable for infants, children, and adults however, it may need to be diluted for children under 5 years.Contra Indications
Not for intravenous use. Strawberry and Banana flavours are not suitable for children under 3 years of age. Not suitable as a sole source of nutrition. Only to be used as a supplement to the normal diet or in conjunction with other oral nutritional supplements containing vitamins and minerals.
Special Precautions
Must be used under strict medical supervision.Manufacturer
SHSUpdated
15 April 2009Advert for Healthcare Professionals Only
Latest News
12th February 2012
Cyberknife (Accuray Inc) relieves pain of Trigeminal Neuralgia facial nerve condition Page
Cyberknife, the Intensity Modulated RadioTherapy system from Accuray Inc, can relieve the stabbing pain of the facial nerve condition Trigeminal Neuralgia. Researchers treated 17 patients with Trigeminal Neuralgia with Cyberknife radiosurgery between 2007 and 2009. The patients, who were aged between 36 and 90, had had their symptoms for between one and 11 years and had not responded to the available treatment options. The researchers zapped a 6mm length of trigeminal nerve, just 2 to 3mm from the root, using a maximum radiation dose of 73.06 Gy. The patients were then monitored regularly after the procedure, for an average of just under 12 months. Complete data were available for 16 patients, 14 of whom obtained either partial or complete relief from their symptoms. The average time before symptom relief occurred was just under two months, but varied from three weeks to six months. Four patients relapsed after the procedure, between three and 18 months later. No patient experienced major complications as a result of the procedure, and only two patients reported any sensory side effects. See: >"Cyberknife radiosurgery in treating trigeminal neuralgia" by Bryan M Lazzara et al. Journal of NeuroInterventional Surgery (2012). doi:10.1136/neurintsurg-2011-010125
FDA approves trial of Celution System (Cytori Therapeutics) for CMI Cardiology Page
Cytori Therapeutics has received an Investigational Device Exemption (IDE) approval from the FDA to begin the ATHENA trial using its Celution System. ATHENA will investigate the use of the Celution System to treat a form of Coronary Heart Disease, Chronic Myocardial Ischemia (CMI). The IDE application was originally submitted to the FDA in December 2011. The trial will enroll up to 45 patients with no-option CMI who have limited therapeutic options. It will evaluate a variety of clinical and functional outcomes, including safety, peak oxygen consumption (mVO2), and clinical outcomes at 12-months.
Phase III Trial of MDV 3100 (Medivation/Astellas) in Prostate Cancer patients shows positive results Oncology Page
Researchers have presented positive results on all efficacy endpoints from the Phase III AFFIRM trial of the investigational drug MDV 3100, from Medivation and Astellas, in men with Prostate Cancer previously treated with chemotherapy. The results, presented at the 2012 Genitourinary Cancers Symposium, show that men taking MDV 3100 lived for a median of 18.4 months, compared with 13.6 months for men taking placebo. MDV 3100 also met all secondary endpoints, including radiographic progression-free survival (8.3 versus 2.9 months; PSA declines of 50% or greater were more common in the MDV 3100 group than in the placebo group (54.0% versus 1.5%; and MDV 3100 was found to be well tolerated. The data was presented by Howard I. Scher, chief, Genitourinary Oncology Service at Memorial-Sloan Kettering Cancer Center.
