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
121989934 12198993 4 F 20160826 20160322 20160909 EXP GB-TEVA-644257ACC TEVA 0.00 M Y 132.00000 KG 20160909 MD 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
121989934 12198993 1 PS RAMIPRIL. RAMIPRIL 1 Unknown 019151 77470 10 MG CAPSULE

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
121989934 12198993 OT
121989934 12198993 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121989934 12198993 Asthenia
121989934 12198993 Feeling abnormal
121989934 12198993 Feeling of body temperature change
121989934 12198993 Hypoaesthesia
121989934 12198993 Insomnia
121989934 12198993 Sensory loss
121989934 12198993 Speech disorder

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
121989934 12198993 1 20130204 0