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
127620761 12762076 1 I 20160823 20160912 20160920 20160920 EXP GB-MHRA-EYC 00144843 GB-DRREDDYS-GER/UKI/16/0083257 DR REDDYS 32.00 YR F Y 77.00000 KG 20160920 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
127620761 12762076 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 1000 MG N U UNKNOWN 75593 500 MG BID
127620761 12762076 2 C METRONIDAZOLE. METRONIDAZOLE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127620761 12762076 1 Product used for unknown indication
127620761 12762076 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127620761 12762076 OT
127620761 12762076 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127620761 12762076 Muscle twitching
127620761 12762076 Myalgia
127620761 12762076 Nightmare
127620761 12762076 Pain in extremity
127620761 12762076 Paraesthesia
127620761 12762076 Tendon pain

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
127620761 12762076 1 20160823 20160824 0