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
126646812 12664681 2 F 20160803 20160819 20160818 20160824 EXP GB-SA-2016SA150235 AVENTIS 87.00 YR E F Y 0.00000 20160824 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
126646812 12664681 1 SS RAMIPRIL. RAMIPRIL 1 Unknown U UNKNOWN 0 5 MG
126646812 12664681 2 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 Unknown U UNKNOWN 0 10 MG
126646812 12664681 3 PS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Unknown U UNKNOWN 20839 75 MG
126646812 12664681 4 SS LYRICA PREGABALIN 1 Unknown U UNKNOWN 0 150 MG
126646812 12664681 5 SS AMITRIPTYLINE AMITRIPTYLINE 1 Unknown U UNKNOWN 0 100 MG
126646812 12664681 6 SS RANITIDINE. RANITIDINE 1 Unknown U UNKNOWN 0 300 MG
126646812 12664681 7 SS LACTULOSE. LACTULOSE 1 Unknown U UNKNOWN 0 15 ML

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126646812 12664681 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126646812 12664681 Contusion
126646812 12664681 Diarrhoea
126646812 12664681 Loss of consciousness
126646812 12664681 Skin abrasion

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

no results found

Therapies reported

no results found