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GRIFULVIN V Tablet ; GRISEOFULVIN ULTRAMICROSIzE GRIS-PEG GYNAzOLE-1 MONISTAT 7 COMBINATION PA SPORANOx Kit ; SPORANOx Solution ; TERAzOL 3 Suppository ; VFEND VFEND I.V. Generics amphocin amphotericin b clotrimazole eq miconazole 3 combo pac eq tioconazole 1 fluconazole 100mg tablet, 200mg. 483.410 c ; 3 ; FACILITY PRACTICES: The facility has developed the required policies and procedures and follows them. Release of any personally identifiable information does not occur unless appropriate consent s ; is obtained prior to the release. 483.410 c ; 3 ; GUIDELINES: Although one facet of the requirement is that the facility must decide how this is to be accomplished i.e., policies and procedures ; , the surveyor's primary focus should be on the second part of the requirement, i.e., the facility's implementation or "outcome" that consent is obtained prior to the release of any individual information e.g., records, photographs, interviews, or other means of exposure to public view or identification ; . The following guidance is provided to assist in determining whether informed consent for release of information is adequate: 1. Was the confidential information to be released specifically identified? 2. Was the person or agency to whom the information was to be released identified to the consenting party? 3. Was the consent time-limited i.e., include the date the consent was given, and the date which the specific consent would be invalid ; ? 4. Was the person giving consent legally able to give consent? Information regarding an individual's HIV status may not be released without specific consent and may not be in the record if that consent has not been given. Staff are expected to use universal precautions when dealing with all individuals, therefore, it is unnecessary to routinely share information about HIV status with all staff. Under some conditions, knowledge may be shared with those directly involved in the care of infected persons. Surveyors should be familiar with State law requirements. 483.410 c ; 4 ; GUIDELINES: In cases in which facilities have created the option for an individual's record to be maintained by computer, rather than hard copy, electronic signatures are acceptable. Given the large number of entries that are made in individual's records, this requirement is cited only when a systemic problem is identified, for example, how long does it take for fluconazole to work. You may not be able to take fluconazole, or you may require a dosage adjustment or special monitoring during treatment if you are taking any of the medicines listed above. Product Vincristine Albuterol Alprozalam Felodipine Fljconazole Norfloxacin Doxazosin Omeprazole Alendronate Sertraline Flutamide Ciprofloxacin Olanzapine Cetirizine Expiry Oct 2003 Expired Expired Dec 2001 Jan 2004 Nov 2003 Expired Expired Aug 2007 Dec 2005 Expired Dec 2003 2011 Jun 2007 Sales Mn ; $300 $450 $1010 $500 $800 $6300 $1050 $2140 $200 $1650 $2370 $600 Date of filing DMF by Cipla 28 Jul 1986 20 Jan 1978 06 May 1989 17 Apr 1995 17 Apr 1995 15 Jan 1996 12 Dec 1997 21 Jan 1998 06 Aug 1999 05 Oct 1999 20 Dec 1999 11 Feb 2000 18 Sep 2000 17 Nov 2000 Expected Launch Launched Started Supplying Launched Supply expected by end of Dec 2001 Launch expected by end of Dec 2003 Launched Expected by Q2 CY02 Supply expected by Q1 CY06 Started Supplying Expected launch by H2 CY04 Expected to launch by CY04 Alliance Ivax Ivax Andrx Ivax Ivax . Ivax Comment Very old product. Very Old Product No competition. However, very old and matured product 5 generic players. 7 generic players No competition as of now. Matured Product, 8 generic players Andrx has received 180-dyas exclusivity One DMF filed by another generic player No other DMF filed as of now Many generic players Many generic players Patent is under challenge. One more generic player. 2 more generic players.
Funding: The study was sponsored by LEPRA UK, the Leprosy Mission International, the American Leprosy Missions, the University of Aberdeen, and the International Nepal Fellowship. Competing interests: None declared. Ethical approval: The study design was reviewed by the medical advisory board of LEPRA and the technical and ethical standards committee of the International Nepal Fellowship. The Nepal Health Research Council and the Bangladesh Medical Research Council gave ethical approval.
Antifungal agents, including Amphotericin B; Fluconazole; Itraconazole; Ketoconazole Anti-cancer drugs Vinblastine; Etoposide; Bleomycin; Vincristine 1. Dossier evaluation. Dossiers were thoroughly evaluated for compliance with WHO recommendations and guidelines regarding the assessment of Multisource products "Marketing Authorization of Pharmaceutical Products with special Reference to Multisource Generic ; Products: a Manual for a Drug Regulatory Authority, WHO DMP RGS 98.5 ; and bioequivalence data Annex 9, WHO Technical Report Series No 863 ; , and ICH guidelines where appropriate to complement the aforesaid WHO recommendations and guidelines. Each product dossier was evaluated by a team of evaluators three for quality aspects, two for bioavailability bioequivalence ; . Suppliers were informed of the outcome of the evaluation and were given the opportunity to submit additional data and information requested. To date, 243 product dossiers for various products and dosage forms from 34 suppliers were received. Some dossiers have now been fully evaluated and all the required data and information have been submitted. Those products that were found to comply with the standards referred to above, have been included in the list. Several suppliers are currently still generating additional data and information on their products as part of the assessment process. In addition, new products may be submitted to WHO for evaluation. If and when products are found to meet the specified standards, they will be added to the list and galantamine.
Although itraconazole, fluconazole and terbinafine are commonly referred to as "newer" oral antifungal agents, this categorization is based on the conspicuous absence of additional agents, especially for cutaneous indications, since 1996. With regard to treatment of onychomycosis and other cutaneous uses, itraconazole and terbinafine are "time tested" in terms of efficacy and safety, with a continuous accumulation of clinical experience in several million patients.
Admission blood work was remarkable for a normal cell count and differential, hemoglobin of 7.1 g dL, and platelets of 640, 000 L. The biochemistry profile and liver enzyme findings were normal. Chest radiography showed a round opacity with adjacent airspace disease in the right lower lobe Fig 1 ; . Subsequent testing included a nonreactive tuberculin skin test, negative fungal serology results, negative serum cryptococcal antigen, and a negative HIV screen. A CT-guided, fine-needle aspiration of the parenchymal lesion was performed. Direct smear showed "few fungal elements" and mixed inflammatory cells. Seventeen days later, fungal cultures grew Cryptococcus neoformans. Infliximab therapy was discontinued. The patient was treated with amphotericin-B, followed by fluconazole maintenance therapy, with significant improvement of respiratory symptoms and glibenclamide!
The performance of the algorithm is tested at 915 MHz using our Smart Antenna Software RAdio Test System SASRATS ; platform [4, 14] and the Hewlett Packard HP ; 11759B radio frequency RF ; channel simulator. SASRATS was designed and developed as a functional and flexible system to facilitate the testing of space-time processing architectures and algorithms at 915 MHz. It also facilitates the correlation between simulated and measured performance. In this paper, due to limitations of the HP RF channel simulator, the SASRATS platform is configured as a 1 and 2 RX SIMO system. The 915 MHz transmitter is modulated with BPSK signals at 20 KBaud which corresponds to a symbol period of 50 uS. The output of the transmitter is split into two equal paths and fed into the two inputs of HP channel simulator. The two outputs of the channel simulator are then fed into 2 SASRAT receivers. The output of the SASRAT receivers consist of symbol sampled complex baseband signals which is then processed in Matlab. For each experiment there are 100 independent trials and each trial consist of 1000 BPSK symbols. The HP RF channel simulator has 2 separate channels and there are 3 programmable paths in each channel. In this experiment, each path is programmed with various delays and attenuation levels as outlined in Table 3. There are two.
Nonunion and nonunion complicated by subclinical osteomyelitis because of the increased tracer activity associated with new bone formation at the nonunion site. M.ta-Iodobenzylguanidine Adrenal Medulla Localization: Auto radIographic and Pharmacologic Studies. D. Guilloteau, J.-L and glucovance.
Additional monitoring of your dosage or condition may be needed if you are taking amiodarone, blood thinners such as warfarin, bosentan, cyclosporine, dalfopristin or quinupristin, digoxin, diltiazem, fluconazole, imatinib, rifamycins such as rifampin, st. Why are drug prices unpredictable? and inderal. FLOXIN OTIC, 56 fluconazole, 17, 41 fludrocortisone, 37 FLUMADINE, 19 fluocinolone acetonide crm, oint 0.025%, 51 fluocinolone acetonide crm, soln 0.01%, 51 fluocinonide crm, gel, oint 0.05%, 52 fluoride drops, 45 fluoride tabs, 45 fluorometholone, 54 fluorometholone 0.25%, 54 FLUOROPLEX, 50 fluorouracil crm 1%, 50 fluorouracil soln 2%, 5%, 50 flutamide, 20 fluticasone, 49 fluticasone spray, 48 fluticasone salmeterol, 49 FML, 54 FML FORTE, 54 FML-S, 54 folic acid, 45 FORADIL AEROLIZER, 48 formoterol inhalation caps, 48 FORTEO, 37 FORTOVASE, 18 FOSAMAX, 33 FOSAMAX PLUS D, 33 fosamprenavir, 18 fosinopril, 22 fosinopril hydrochlorothiazide, 22 FOSRENOL, 37 furosemide, 26.
PATIENT ADHERENCE WITH LONG-TERM PROTON PUMP INHIBITOR THERAPY IN A VETERAN POPULATION Priya K Patel * , Latoya E Bernard, John Inadomi, Lisa McIntyre VA Ann Arbor Healthcare System, 2215 Fuller Rd 119 ; , Ann Arbor, MI, 48105 priyakp umich Background: Prescribing of proton pump inhibitors PPIs ; has increased dramatically since their advent and is a major contributor to ever increasing medication expenditures. Attempts to decrease medication expenditures have resulted in the development of novel methods of PPI use, which may prove to be the most efficacious and cost-effective in a subset of patients. Other studies that have assessed patient adherence with long-term PPI have been conducted in the U.K. within the general practice setting. The VA provides a unique setting with a unique population and thus previous data from these other regions cannot be extrapolated to the VA healthcare system. The high use and cost of PPIs at VAAAHS necessitates the assessment of adherence in this patient population. Objectives: The primary objective of this study is to assess patient adherence with long-term PPI therapy at the VA Ann Arbor Healthcare System VAAAHS ; . Secondary objectives are to determine indications for long-term PPI therapy and factors predictive of adherence. Methods: All patients with a PPI prescription for greater than eight weeks at the VAAAHS between August 1, 2001 and July 31, 2003 will be identified from computerized prescription databases. A subset of 1500 patients will be randomly selected from this list for inclusion in the study. Prescription information gathered from the computerized pharmacy database will include prescription number, drug, dose, directions, quantity, refills, start date, last fill date, and stop date. Following this, electronic patient charts will be reviewed in CPRS DHCP to gather information on demographics, indications, prescribing physician specialty, and active concurrent medications. The data will then be analyzed to assess adherence, determine indications, and ascertain factors predictive of adherence. Results Conclusions: In progress Learning Objectives: Assess patient adherence with long-term proton pump inhibitor therapy. Determine indications for long-term PPI therapy and factors predictive of adherence. Self Assessment Questions: The majority 50% ; of VAAAHS patients use on-demand PPI therapy. T or F Demographic characteristics age gender ethnicity marital status ; are not good predictors of adherence. T or F and itraconazole.
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Project Description The current socio-economic crisis in Zimbabwe has worsened the plight of children, especially under fives. About 70% of children under five years of age die from a few manageable conditions; namely acute respiratory infections, diarrhoea, malaria, malnutrition with HIV AIDS being an important underlying cause. It has however been shown that a significant reduction in morbidity and mortality can be obtained by using intervention strategies, notably the integrated management of childhood illness IMCI ; strategy, which has given a reduction in morbidity and mortality of up to 70% in recent studies carried out. Strengthening of health worker skills, adequate supplies of essential drugs and equipment and proper home care practices are therefore of paramount importance in reducing Under Five morbidity and mortality. The use of the abridged IMCI training course is thus proposed. Relation to CHAP Strategic and Short-term goals and sector objectives The project is in line with the overall Health Sector goal of improving and maintaining minimum basic health services in order to reduce morbidity and mortality in vulnerable populations. It also fits in with the first two objectives of the plan i.e. a ; To deliver minimum health services to vulnerable populations, and b ; To improve and maintain the capacity of the health system to respond to humanitarian crisis in the vulnerable populations Expected Outcome The main expected outcome would be improved ability to recognise and manage common fatal Under Five conditions. Improved essential drugs and equipment requirements, better pre-referral and referral care practices and better home care practices are also expected at the end of the project. Financial Summary A total of US$ 431, 420 is being requested to ensure immediate Health Worker skills training and follow up, to obtain essential drugs and medical supplies and for monitoring and evaluation of the project. The cost is inclusive of fuel and stationery costs, for instance, c fluconazole.
Removed from restraints placed on floor cpr started immediately -- emergency help called. Fire Dept. responded. Medical Doctor and Psych Doctor -- Hospital Police also responded." Upon arriving at the death scene, paramedics noted that Jadeed's skin was moist, pale and cyanotic turning blue from lack of oxygen his temperature was cool; his pupils were dilated and fixed. He was unresponsive and not breathing. The fire department continued CPR until Jadeed was pronounced dead. At 10: 50 PM, after Dr. C arrived, Jadeed was intubated and given Epinephrine 1 mg. intravenously. A suction tube was used to clear vomit out of the endotracheal tube. Dr. C could find no pulse rate, no respiratory rate, and no muscle or pupil reflexes. At approximately 10: 52 PM, March 15, 1992, Dr. C pronounced Zouhair Jadeed dead and ketoconazole.
Infectious disease department, ullevl university hospital, oslo, norway; medical department, rikshospitalet, oslo, norway; pharmaceutical institute, rigshospitalet, copenhagen, denmark; department of gastroenterology, malm university hospital, malm, sweden.
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Fluconazole tablet for ringwormSolution. Itraconazole represents an advance beyond earlier therapies due to its broad spectrum of activity, its high affinity for keratin 16 ; , and its pharmacokinetic profile. Itraconazole is rapidly absorbed, with peak levels attained within 4 h. It subject to extensive first-pass metabolism and has a maximal oral bioavailability of about 56%. Peak levels in plasma of 0.127 and 0.272 g ml are reached after a single oral dose of 100 or 200 mg, respectively. Steady-state concentrations are reached after 10 to 14 days of dosing and are three to four times higher than after a single dose. Itraconazole has a high affinity for proteins, and 99.8% of the circulating compound is bound to plasma proteins. However, the distribution of itraconazole in tissues is considerably higher, and the tissue plasma concentration ratio ranges from 1: in the brain to 25: 1 in fat 16 ; . Itraconazole is rapidly eliminated from the systemic circulation within 7 to 10 days and is excreted in the urine 35% ; and feces 54% ; . Itraconazole reaches the site of infection within 24 h of administration and can be detected in the distal nail plate as soon as 1 month after the beginning of therapy 46 ; . The rapid diffusion into the distal nail indicates that itraconazole penetrates the nail unit via the nail bed, which is confirmed by the twofold-higher drug levels in subungual nail material than in distal nail clippings of a patient treated with this drug for 1 month 16 ; . An early analysis of the kinetics of itraconazole penetration demonstrated the persistence of high drug levels in fingernails and toenails after the cessation of therapy Fig. 9 ; 53 ; . can be seen in Fig. 8, itraconazole persists in the nail for longer than fluconazole or terbinafine and can be detected for as long as 9 months 16 ; . Mean maximal itraconazole levels in toenails in two published studies were 149 ng g after a 100-mg dose and 99 ng g after a 200-mg dose; the corresponding values for levels in fingernails were 111 and 80 ng g, respectively 16 ; . Concentrations in toenails remain elevated longer than do those in fingernails after cessation of therapy. By contrast, levels of itraconazole in plasma decrease rapidly and the compound is completely eliminated 1 week after a pulse dose 16 ; . Although initially indicated for the treatment of onychomycosis due to dermatophytes, itraconazole may also be effective in nondermatophytic infections. For example, one study involved 36 patients with toenail onychomycosis caused by nondermatophyte molds alone or in combination with dermatophytes. Patients received itraconazole as continuous therapy or as a one-week pulse regimen. At 12 months follow-up, clinical and mycologic cures were seen in 88% of the patients whose infections were caused by a single mold 17 ; . Evidence from several clinical trials supports the effective.
The purpose of this study was to assess the effect of voriconazole on the blood tacrolimus concentration in a liver transplant recipient and to examine the interaction between voriconazole and tacrolimus by using human liver microsomes. Two subjects were enrolled in the clinical study: one received voriconazole, and the other received a placebo. Tacrolimus metabolism was evaluated in human liver microsomes at various concentrations in the absence and presence of various concentrations of voriconazole. Coadministration of voriconazole and tacrolimus resulted in elevated nearly 10-fold-higher ; trough tacrolimus blood concentrations in the liver transplant patient. In the in vitro study, voriconazole at a concentration of 10.4 4.3 g ml inhibited the metabolism of tacrolimus by 50%. Clinically relevant concentrations of voriconazole inhibited the metabolism of tacrolimus in human liver microsomes. Close monitoring of the blood concentration and adjustment in the dose of tacrolimus are warranted in transplant recipients treated with voriconazole. Organ transplant patients are susceptible to invasive fungal infections that necessitate treatment with antifungal agents including the azoles 9 ; . Azole antifungal agents, e.g., ketoconazole, itraconazole, and fluconazole, are known to inhibit the metabolism of immunosuppressive drugs such as cyclosporine and tacrolimus 7, 8, 12 ; . Voriconazole is a triazole antifungal agent that is currently undergoing phase III clinical trials for the treatment of a variety of fungal infections. Voriconazole is 4- to 16-fold more active than tluconazole and 2- to 8-fold more active than itraconazole against Candida species, including C. krusei and C. glabrata 1, 2, 10 ; . Voriconazole is active against a wide range of filamentous fungi including Aspergillus species. In a randomized trial, voriconazole was more effective than amphotericin B as primary therapy for the treatment of invasive aspergillosis R. Herbrecht et al., Abstr. 41st Intersci. Conf. Antimicrob. Agents Chemother., abstr. J-680, p. 378, 2001 ; . Voriconazole also appears to be a promising agent for the treatment of mycelial fungi that either are innately resistant or respond erratically to amphotericin B, such as hyaline molds and dematiaceous fungi. Availability in an intravenous and a highly bioavailable oral formulation renders voriconazole a potentially valuable drug for the treatment of invasive mycoses in transplant recipients. Antifungal agents are known to inhibit cytochrome P450 3A4 5 CYP3A4 5 ; enzymes. CYP3A4 5 is also involved in the metabolism of cyclosporine, tacrolimus, and sirolimus 3, 11, 13 ; . Preliminary observations indicate that voriconazole at a dose of 200 mg twice a day increases the trough concentrations in blood of cyclosporine in transplant patients P. Ghahramani, A. J. Romero, A. F. Lant, and M. J. Allen, Abstr. 40th Intersci. Conf. Antimicrob. Agents Chemother., abstr. 845, p. 24, 2000 ; . We hypothesized that voriconazole will alter the hepatic metabolism of tacrolimus as well. The objectives of the present study were to evaluate the interaction between voriconazole and lansoprazole and fluconazole. | Fluconazole greenstoneIn addition, the elderly patient may be taking medications that can cause depressive symptoms and levofloxacin. Ing, socks and underwear should be washed on a hot wash cycle.There is no need to avoid sports but sports clothes should be washed regularly and towels should not be shared. Candidal balanitis Balanitis is inflammation of the head of the penis. Although it has many causes, infection with the yeast Candida albicans is the most common.Typically, this presents as generalised erythema of the glans or foreskin, or both which may have a dry glazed appearance ; , with eroded white papules and a white, foulsmelling discharge. Other symptoms include soreness and irritation. Candidal balanitis can be acquired through intercourse with an infected partner but it can also occur in people with diabetes and after antibiotic treatment. Intercourse should be avoided during treatment to avoid reinfection. Topical imidazoles are the first line treatment for candidal balanitis. The cream or ointment should be applied twice daily for two weeks and for at least one week after symptoms have disappeared. A topical imidazole combined with 1 per cent hydrocortisone may be prescribed if there is significant inflammation and itching. Oral flcuonazole is an option if topical treatment is ineffective. Over-the-counter packs of fluconaaole should only be sold for balanitis if recommended by a doctor. Bathing with saline is soothing and may be helpful. Although balanitis is less common in those who have been circumcised, there are no trial data on circumcision as a treatment for recurrent balanitis. For uncircumcised men, good personal hygiene is important to avoid infection -- the area under the foreskin should be kept clean and dry.The consensus view is that circumcision may benefit individuals with recurrent infective balanitis. Acute orofacial pain may be caused by infective, traumatic, neuropathic, vascular, neoplastic or other pathologies Zakrzewska & Harrison 2003; Keith 2004; Ward & Levin 2004 ; . Most commonly, acute orofacial pain is due to dental or sinus disease but it may also be associated with chronic facial pain syndromes eg trigeminal neuralgia ; or be referred from adjacent regions such as the cervical spine and the thorax. A thorough history including dental ; and examination particularly of the oral cavity and cranial nerves ; is vital in the assessment of orofacial pain. Recurrent or persistent orofacial pain requires a biopsychosocial assessment and appropriate multidisciplinary management Vickers et al 2000 ; . Neuropathic orofacial pain atypical odontalgia, phantom pain ; may be exacerbated by repeated dental procedures eg extraction of teeth, root canal therapy, sectioning of nerves ; , incorrect drug therapy or psychological factors Vickers et al 1998. |
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Fluconazole 50mg 5ml Oral Suspension Fkuconazole 200mg 5ml Oral Suspension Flucoanzole 2mg ml in Normal Saline 0.9% 25ml bottle I.V infusion, Electrolyte Na + 15mmol 100ml bottle. ; Fluconazolw 2mg ml in Normal Saline 0.9% 100ml bottle I.V infusion, Electrolyte Na + 15mmol 100ml bottle. ; Griseofulvin 125mg 5ml, Suspension Griseofulvin 125mg Tablet Griseofulvin 500mg Tablet Itroconazole 100mg Capsule Ketoconazole 200mg Tablet Ketoconazole 20mg ml Syrup Miconazole 250 mg Tablet Miconazole 10mg ml I.V. Injection Nystatin 500000 U Tablet Nystatin 100000 U ml Suspension Nystatin 100000 U Pastilles. Organizations in pursuing international efforts for the total eradication of apartheid and support for the establishment of a united, non-racial and democratic South Africa; and to follow the guidelines set for action by the United Nations system in this connection in General Assembly resolution 46 79A and other relevant General Assembly resolutions on South Africa; 6. Authorizes the Director-General to contribute to any United Nations systemwide efforts to provide urgent assistance to the people of South Africa and their anti-apartheid, democratic organizations that may be undertaken during the period of transition towards a non-racial democracy; Expresses its support for the current negotiations involving the representatives of the people of South Africa, in keeping with the fundamental principles set forth in the United Nations Declaration on Apartheid and its Destructive Consequences in Southern Africa; and expreses its hope that South Africa may in the future become a truly free, democratic, non-racial and united society and be able to take its place among the community of nations once again. 139 EX SR.l and 7. Traditional medicines, patient outcome. Trans R Soc Trop Med Hyg. 2006 Jun; 100 6 ; : 515-20 3. Makundi EA, Malebo HM, Mhame P, Kitua AY, Warsame M. Role of traditional healers in the management of severe malaria among children below five years of age: the case of Kilosa and Handeni Districts, Tanzania. Malar J. 2006 Jul 18; 5: 58 : pubmedcentral.nih.gov picrender.fcgi?artid 1540433&blobtype pdf 4. Malik EM, Hanafi K, Ali SH, Ahmed ES, Mohamed KA. Treatment-seeking behaviour for malaria in children under five years of age: implication for home management in rural areas with high seasonal transmission in Sudan. Malar J. 2006 Jul 22; 5: 60 : pubmedcentral.nih.gov picrender.fcgi?artid 1569850&blobtype pdf 5. Okeke TA, Okafor HU, Uzochukwu BS. Traditional healers in Nigeria: perception of cause, treatment and referral practices for severe malaria. J Biosoc Sci. 2006 Jul; 38 4 ; : 491-500 6. Ahorlu CK, Koram KA, Ahorlu C, de Savigny D, Weiss MG. Community concepts of malaria-related illness with and without convulsions in southern Ghana. Malar J. 2005 Sep 27; 4: 47 : pubmedcentral.nih.gov picrender.fcgi?artid 1262759&blobtype pdf 7. Pilkington H, Mayombo J, Aubouy N, Deloron P. Malaria, from natural to supernatural: a qualitative study of mothers' reactions to fever Dienga, Gabon ; . J Epidemiol Community Health 2004 Oct; 58 10 ; : 826-30 8. Winch PJ, Makemba AM, Kamazima SR, Lurie M, Lwihula GK, Premji Z, Minjas JN, Shiff CJ. Local terminology for febrile illnesses in Bagamoyo District, Tanzania and its impact on the design of a community-based malaria control programme. Soc Sci Med. 1996 Apr; 42 7 ; : 1057-67.
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