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
127058041 12705804 1 I 20160615 20160818 20160901 20160901 EXP GB-AUROBINDO-AUR-APL-2016-10773 AUROBINDO 48.00 YR M Y 80.00000 KG 20160901 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
127058041 12705804 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, TWO TIMES A DAY 5000 MG N U 77859 500 MG BID
127058041 12705804 2 C AUGMENTIN AMOXICILLINCLAVULANATE POTASSIUM 1 Unknown U 0
127058041 12705804 3 C DOXYCYCLINE. DOXYCYCLINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127058041 12705804 1 Diverticulitis
127058041 12705804 2 Product used for unknown indication
127058041 12705804 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127058041 12705804 DS
127058041 12705804 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127058041 12705804 Anxiety
127058041 12705804 Arthritis
127058041 12705804 Burning sensation
127058041 12705804 Diarrhoea
127058041 12705804 Dyspnoea
127058041 12705804 Gastrointestinal disorder
127058041 12705804 Insomnia
127058041 12705804 Intervertebral disc disorder
127058041 12705804 Nausea
127058041 12705804 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
127058041 12705804 1 20160610 20160615 0