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
126990931 12699093 1 I 20160615 20160818 20160830 20160830 EXP GB-MHRA-EYC 00143782 GB-DRREDDYS-GER/UKI/16/0082604 DR REDDYS 48.00 YR M Y 80.00000 KG 20160830 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
126990931 12699093 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 5000 MG N U UNKNOWN 75593 500 MG BID
126990931 12699093 2 C AUGMENTIN AMOXICILLINCLAVULANATE POTASSIUM 1 0
126990931 12699093 3 C DOXYCYCLINE. DOXYCYCLINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126990931 12699093 1 Diverticulitis
126990931 12699093 2 Product used for unknown indication
126990931 12699093 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126990931 12699093 DS
126990931 12699093 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126990931 12699093 Anxiety
126990931 12699093 Arthritis
126990931 12699093 Asthenia
126990931 12699093 Burning sensation
126990931 12699093 Diarrhoea
126990931 12699093 Dyspnoea
126990931 12699093 Gastrointestinal disorder
126990931 12699093 Insomnia
126990931 12699093 Intervertebral disc disorder
126990931 12699093 Nausea
126990931 12699093 Tendonitis

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
126990931 12699093 1 20160610 20160615 0