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
125353561 12535356 1 I 201403 20160705 20160707 20160707 EXP FR-ROCHE-1789339 ROCHE 51.00 YR F Y 0.00000 20160707 CN FR FR

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
125353561 12535356 1 PS RIVOTRIL CLONAZEPAM 1 Oral N 17533 45 GTT
125353561 12535356 2 SS RIVOTRIL CLONAZEPAM 1 Oral N 17533 3 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125353561 12535356 1 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
125353561 12535356 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125353561 12535356 Abnormal behaviour
125353561 12535356 Food craving
125353561 12535356 Hallucination
125353561 12535356 Hypoacusis
125353561 12535356 Malaise
125353561 12535356 Memory impairment
125353561 12535356 Pain
125353561 12535356 Pruritus
125353561 12535356 Sleep disorder
125353561 12535356 Suicide attempt

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
125353561 12535356 1 1986 2014 0
125353561 12535356 2 2014 0