Medical Adverse Drug Reaction Information System/ADRIS
Medical Adverse Drug Reaction Information System (ADRIS)
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Posted By Suspected Drug Suspected BrandPosted On
Dr Chandra Mohan KumarArteetherDuther1/17/2009
Dr neeta Kumarparacetamolcalpol1/8/2009
Dr R S SandhumetoclopramidePerinorm7/25/2008
Dr.Vinod GandhiTyphoid vaccineShantyph6/15/2008
dr anil mokashicodeinecorex4/14/2008
dr amit agrawalmeropenemMeronem4/12/2008
luis Alberto Carvajal ViloriaMetronidazole, Trimethoprim sulfamethoxazole 2/26/2008
sahana sunilValproate, Isoniazid, Rifampicin 2/19/2008
Dr Ira ShahPyrazinamide 2/13/2008
yogesh daveCeftriaxone 12/16/2007
Dr. N. D. Vaswaniacycloviracyclovir11/3/2007
AYUSH MANCHANDAPhenytoinPhenytoin11/3/2007
Dr.Santosh singh.CeftriaxoneCeftriaxone10/27/2007
dr.pravin ladCeftriaxone 10/20/2007
Dr T WALICarbamazepineCarbamazepine10/12/2007
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This system has been established to determine unknown adverse effects of drugs so that effective action can be undertaken if the cause and effect can be established. This ADR monitoring program is voluntary and depends on your co-operation to accurately report adverse drug reactions. A simple online form is all that needs to be filled and then the matter will be displayed on the website.

How common are adverse drug reactions?

ADRs are responsible for 5% of hospital admissions
.7% of hospital patients suffer ‘serious' ADRs
0.1 - 0.3% of hospital patients suffer fatal ADRs
ADRs were between the fourth and sixth leading cause of death in the USA in 1994

The vast majority of reports on which the listing is based represents the suspicion, opinion or observation of the individual reporter. Cause and effect relationships have not been established in the vast majority of reports submitted.
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