TY - JOUR
T1 - Pattern of adverse drug reactions notified by spontaneous reporting in an Indian tertiary care teaching hospital
AU - Jose, J.
AU - Rao, P.G.M.
N1 - Cited By :75
Export Date: 10 November 2017
CODEN: PHMRE
Correspondence Address: Jose, J.; Department of Pharmacy Practice, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, 576 104 Karnataka, India; email: [email protected]
Chemicals/CAS: acetylsalicylic acid, 493-53-8, 50-78-2, 53663-74-4, 53664-49-6, 63781-77-1; amlodipine, 88150-42-9; amoxicillin, 26787-78-0, 34642-77-8, 61336-70-7; cyclophosphamide, 50-18-0; doxorubicin, 23214-92-8, 25316-40-9; gabapentin, 60142-96-3; heparin, 37187-54-5, 8057-48-5, 8065-01-8, 9005-48-5; ibuprofen, 15687-27-1; isoniazid, 54-85-3, 62229-51-0, 65979-32-0; levofloxacin, 100986-85-4, 138199-71-0; lorazepam, 846-49-1; methotrexate, 15475-56-6, 59-05-2, 7413-34-5; phenytoin, 57-41-0, 630-93-3; prednisone, 53-03-2; salbutamol, 18559-94-9; theophylline, 58-55-9, 5967-84-0, 8055-07-0, 8061-56-1, 99007-19-9; warfarin, 129-06-6, 2610-86-8, 3324-63-8, 5543-58-8, 81-81-2; Antineoplastic Agents; Pharmaceutical Preparations; Phenytoin, 57-41-0
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Estimate based on a spontaneous reporting scheme and a sentinel system (1998) Eur J Clin Pharmacol, 54, pp. 483-488; Gallelli, L., Ferreri, G., Colosimo, M., Pirritano, D., Flocco, M.A., Pelaia, G., Retrospective analysis of adverse drug reactions to bronchodilators observed in two pulmonary divisions of Catanzaro, Italy (2003) Pharmacol Res, 47 (6), pp. 493-499; Wu, W.K., Evaluation of outpatient adverse drug reactions leading to hospitalization (2003) Am J Health-Syst Pharm, 60 (3), pp. 253-259; Regal, B., Finally a pharmacovigilant India (2004) Uppsala Rep, 25, pp. 7-8; Adithan, C., National pharmacovigilance program (2005) Indian J Pharmacol, 37, p. 347; Gallelli, L., Ferreri, G., Colosimo, M., Pirritano, D., Guadagnino, L., Pelaia, G., Adverse drug reactions to antibiotics observed in two pulmonology divisions of Catanzaro, Italy: a six year retrospective study (2002) Pharmacol Res, 46 (5), pp. 395-400; Rawlins, M.D., Thompson, J.W., Pathogenesis of adverse drug reactions (1977) Textbook of adverse drug reactions. 1st ed., p. 44. , Davies D.M. (Ed), Oxford University Press, Oxford; Naranjo, C.A., Busto, U., Sellers, E.M., Sandor, P., Ruiz, I., Roberts, E.A., A method for estimating the probability of adverse drug reactions (1981) Clin Pharmacol Ther, 30, pp. 239-245; Lau, P.M., Stewart, K., Dooley, M.J., Comment: hospital admissions resulting from preventable adverse drug reactions (2003) Ann Pharmacother, 37, pp. 303-312; Edwards, I.R., Pharmacological basis of adverse drug reactions (1997) Avery's drug treatment. 4th ed., pp. 261-299. , Speight T.M., and Holford N.H.G. (Eds), Adis International, Auckland, New Zealand; Parthasarathi, G., Sten, O., Adverse drug reactions (2004) A text book of clinical pharmacy practice-essential concepts and skills. 1st ed., pp. 86-102. , Parthasarathi G., Nyfort-Hansen K., and Nahata M.C. (Eds), Orient Longman Private Limited, Chennai; Veehof, L.J.G., Stewart, R.E., Haaijer-Ruskamp, F.M., Meyboom-de Jong, B., The development of polypharmacy. A longitudinal study (2000) Family Practice, 17 (3), pp. 261-267; Bates, D.W., Spell, N., Cullen, D.J., Burdick, E., Laird, N., Petersen, L.A., The cost of adverse drug events in hospitalized patients (1997) JAMA, 277, pp. 307-311; Gonzalez-Martin, G., Caroca, C.M., Paris, E., Adverse drug reactions (ADRs) in hospitalized pediatric patients-a prospective study (1998) Int J Clin Pharmacol Ther, 36 (10), pp. 530-533; Impicciatore, P., Choonara, I., Clarkson, A., Provasi, D., Pandolfini, C., Bonati, M., Incidence of adverse drug reactions in paediatric in/out-patients: a systematic review and meta-analysis of prospective studies (2001) Br J Clin Pharmacol, 52 (1), pp. 77-83; Gholami, K., Shalviri, G., Factors associated with preventability, predictability, and severity of adverse drug reactions (1999) Ann Pharmacother, 33 (2), pp. 236-240; Bates, D.W., Cullen, D.J., Laird, N., Petersen, L.A., Small, S.D., Servi, D., Incidence of adverse drug events and potential adverse drug events-implications for prevention (1995) JAMA, 274 (1), pp. 29-34; Bennett, B.S., Lipman, A.G., Comparative study of prospective surveillance and voluntary reporting in determining the incidence of adverse drug reactions (1977) Am J Hosp Pharm, 34, pp. 931-936; Montastruc, J.L., Lapeyre-Mestre, M., Bagheri, H., Fooladi, A., Gender differences in adverse drug reactions: analysis of spontaneous reports to a Regional Pharmacovigilance Centre in France (2002) Fundam Clin Pharmacol, 16 (5), pp. 343-346; Suh, D.C., Woodall, B.S., Shin, S.K., Hermes-De-Santis, E.R., Clinical and economic impact of adverse drug reactions in hospitalized patients (2000) Ann Pharmacother, 34, pp. 1373-1379; Prosser, T.R., Kamysz, P.L., Multidisciplinary adverse drug reaction surveillance program (1990) Am J Hosp Pharm, 47 (6), pp. 1334-1339; Kanjanarat, P., Winterstein, A.G., Johns, T.E., Hatton, R.C., Gonzalez-Rothi, R., Segal, R., Nature of preventable adverse drug events in hospitals: a literature review (2003) Am J Health Syst Pharm, 60, pp. 1750-1759; Bates, D.W., Leape, L.L., Petrycki, S., Incidence and preventability of adverse drug events in hospitalized adults (1993) J Gen Intern Med, 8, pp. 289-294; Gandhi, T.K., Weingart, S.N., Borus, J., Seger, A.C., Peterson, J., Burdick, E., Adverse drug events in ambulatory care (2003) N Eng J Med, 348, pp. 1156-1164; Evans, R.S., Lloyd, J.F., Stoddard, G.J., Neberker, J.R., Samore, M.H., Risk factors for adverse drug events: a 10 year analysis (2005) Ann Pharmacother, 39, pp. 1161-1168; Fonescue, E.B., Kausbal, R., Landrigan, C.P., McKenna, K.J., Clapp, M.D., Federico, F., Prioritizing strategies for preventing medication errors and adverse drug events in pediatric inpatients (2003) Pediatrics, 111 (4 PART 1), pp. 722-729; Field, T.S., Gurwitz, J.H., Avorn, J., McCormick, D., Jain, S., Eckier, M., Risk factors for adverse drug events among nursing home residents (2001) Arch Intern Med, 161, pp. 1629-1634; Bates, D.W., Miller, E.B., Cullen, D.J., Burdick, L., Williams, L., Laird, N., Patient risk factors for adverse drug events in hospitalized patients (1999) Arch Intern Med, 159, pp. 2553-2559
PY - 2006
Y1 - 2006
N2 - Hospital-based adverse drug reaction (ADR) monitoring and reporting programs aims to identify and quantify the risks associated with the use of drugs. The present study was undertaken to characterize the pattern of ADRs reported in a tertiary care teaching hospital (Kasturba Hospital, Manipal) in South India. The study was conducted based on the ADRs reported between March 2004 and February 2005 (12 months) to the ADR reporting unit of the hospital. Evaluation of the data was done for various parameters which included patient demographics, drug and reaction characteristics, and outcome of the reactions. Assessment was also done for causality, severity, preventability, and predisposing factors. A total of 408 ADRs which were reported during the 12 months period were evaluated. The overall incidence of ADR calculated from the patient population was 0.15%. At least one ADR was reported in 1.14% of the hospitalised patients and in 0.012% of the outpatients. No significant difference was seen in the overall incidence of ADRs observed in males and females. Incidence of ADRs among elderly adults and older adults (0.23%) were significantly higher than other age groups. Type A reactions (72.5%) accounted for majority of the reports and a greater share of the ADRs were described to be very common (43.4%) in the literature. Dermatological system (23.5%) was the most commonly affected organ system with skin rash (10.5%) as the most frequently reported reaction. Antineoplastic agents (21.8%) was the drug class most commonly involved, while phenytoin (7.8%) was the individual drug most frequently reported. The suspected drug was withdrawn for the management of the ADR in majority (56.6%) of the reports. In 74.8% of the reports the patient recovered from the reaction at the time of evaluation. Upon causality assessment, majority of the reports were rated as probable (53.7%). Mild and moderate reactions accounted for 50.5 and 43.9%, respectively. In 28.7% of the reports, the reaction was considered to be preventable. At least one predisposing factor was present in 79.9% of the reports and the most common predisposing factors associated were polypharmacy and multiple disease state. Evaluating the relationship between patient characteristics and reaction characteristics, type A reactions were more common among elderly adults (85.92%) and type B reactions more common in adults (35.01%) compared to other age groups. In conclusion, the pattern of ADRs reported in our hospital is comparable with the results of studies conducted in hospital set up elsewhere. Our evaluations revealed opportunities for interventions especially for the preventable ADRs to ensure safer drug use. © 2006 Elsevier Ltd. All rights reserved.
AB - Hospital-based adverse drug reaction (ADR) monitoring and reporting programs aims to identify and quantify the risks associated with the use of drugs. The present study was undertaken to characterize the pattern of ADRs reported in a tertiary care teaching hospital (Kasturba Hospital, Manipal) in South India. The study was conducted based on the ADRs reported between March 2004 and February 2005 (12 months) to the ADR reporting unit of the hospital. Evaluation of the data was done for various parameters which included patient demographics, drug and reaction characteristics, and outcome of the reactions. Assessment was also done for causality, severity, preventability, and predisposing factors. A total of 408 ADRs which were reported during the 12 months period were evaluated. The overall incidence of ADR calculated from the patient population was 0.15%. At least one ADR was reported in 1.14% of the hospitalised patients and in 0.012% of the outpatients. No significant difference was seen in the overall incidence of ADRs observed in males and females. Incidence of ADRs among elderly adults and older adults (0.23%) were significantly higher than other age groups. Type A reactions (72.5%) accounted for majority of the reports and a greater share of the ADRs were described to be very common (43.4%) in the literature. Dermatological system (23.5%) was the most commonly affected organ system with skin rash (10.5%) as the most frequently reported reaction. Antineoplastic agents (21.8%) was the drug class most commonly involved, while phenytoin (7.8%) was the individual drug most frequently reported. The suspected drug was withdrawn for the management of the ADR in majority (56.6%) of the reports. In 74.8% of the reports the patient recovered from the reaction at the time of evaluation. Upon causality assessment, majority of the reports were rated as probable (53.7%). Mild and moderate reactions accounted for 50.5 and 43.9%, respectively. In 28.7% of the reports, the reaction was considered to be preventable. At least one predisposing factor was present in 79.9% of the reports and the most common predisposing factors associated were polypharmacy and multiple disease state. Evaluating the relationship between patient characteristics and reaction characteristics, type A reactions were more common among elderly adults (85.92%) and type B reactions more common in adults (35.01%) compared to other age groups. In conclusion, the pattern of ADRs reported in our hospital is comparable with the results of studies conducted in hospital set up elsewhere. Our evaluations revealed opportunities for interventions especially for the preventable ADRs to ensure safer drug use. © 2006 Elsevier Ltd. All rights reserved.
U2 - 10.1016/j.phrs.2006.05.003
DO - 10.1016/j.phrs.2006.05.003
M3 - Article
SN - 1043-6618
VL - 54
SP - 226
EP - 233
JO - Pharmacological Research
JF - Pharmacological Research
IS - 3
ER -