The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126591423 12659142 3 F 20160803 20160824 20160817 20160829 EXP GB-SA-2016SA148567 AVENTIS 87.00 YR E F Y 0.00000 20160829 CN GB GB

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126591423 12659142 1 SS RAMIPRIL. RAMIPRIL 1 Unknown 5 MG, UNK U UNK 0 5 MG
126591423 12659142 2 PS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Unknown 75 MG, UNK U UNK 20839 75 MG
126591423 12659142 3 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 Unknown 10 MG, UNK U UNK 0 10 MG
126591423 12659142 4 SS AMITRIPTYLINE AMITRIPTYLINE 1 Unknown 100 MG, UNK U UNK 0 100 MG
126591423 12659142 5 SS LACTULOSE. LACTULOSE 1 Unknown 15 ML, UNK U UNK 0 15 ML
126591423 12659142 6 SS LYRICA PREGABALIN 1 Unknown 150 MG, UNK U UNK 0 150 MG
126591423 12659142 7 SS RANITIDINE. RANITIDINE 1 Unknown 300 MG, UNK U UNK 0 300 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126591423 12659142 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126591423 12659142 Contusion
126591423 12659142 Diarrhoea
126591423 12659142 Loss of consciousness
126591423 12659142 Skin abrasion

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found