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
127111512 12711151 2 F 20160916 20160902 20160923 EXP GB-MHRA-ADR23609175 GB-BAUSCH-BL-2016-020840 BAUSCH AND LOMB 81.00 YR F Y 0.00000 20160923 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
127111512 12711151 1 PS METRONIDAZOLE. METRONIDAZOLE 1 Unknown N Y 20743 400 MG
127111512 12711151 2 C PARACETAMOL ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127111512 12711151 1 Infection
127111512 12711151 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127111512 12711151 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127111512 12711151 Abdominal pain Abdominal pain
127111512 12711151 Decreased appetite Decreased appetite
127111512 12711151 Diarrhoea Diarrhoea
127111512 12711151 Dysgeusia Dysgeusia
127111512 12711151 Muscular weakness Muscular weakness
127111512 12711151 Nausea Nausea

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
127111512 12711151 1 20160803 20160809 0