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
Nrayan UsgaonkerCarbamazepineCarbamazepine10/2/2007
Dr AtulCrystalline penicillin 10/1/2007
Lavender KalpsAmoxicillin-Clavulanic acidAmoxicillin-Clavulanic acid9/27/2007
Dr Arvindalbendazolealbendazole9/14/2007
dr amar patelloperamideloperamide9/6/2007
Gloria GridleyTopiramate, PhenteramineTopamax , Phentermin9/4/2007
Dr.Tusharkanti SahuCeftriaxoneCeftriaxone7/22/2007
dr naushadondansetronondansetron5/22/2007
Dr Ira ShahSulphonamide 5/19/2007
Dr Ira ShahIsoniazid, Rifampicin, Piperacillin TazobactumMacox ZH Kid, Piptaz5/19/2007
Jasbir S. ChughRIFAMPICIN 5/5/2007
dr.nareshhydrocortisone 4/15/2007
dr.sidharthaCeftriaxone 4/1/2007
Dr Santosh UsgaonkerNorfloxacinNorfloxacin2/24/2007
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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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