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
127027621 12702762 1 I 20160615 20160818 20160831 20160831 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122819 RANBAXY 48.00 YR M Y 80.00000 KG 20160831 OT 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
127027621 12702762 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, BID 5000 MG N U 75747 500 MG Q12H
127027621 12702762 2 C AUGMENTIN AMOXICILLINCLAVULANATE POTASSIUM 1 Unknown UNK U U 0
127027621 12702762 3 C DOXYCYCLINE. DOXYCYCLINE 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127027621 12702762 1 Diverticulitis
127027621 12702762 2 Product used for unknown indication
127027621 12702762 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127027621 12702762 OT
127027621 12702762 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127027621 12702762 Anxiety
127027621 12702762 Arthritis
127027621 12702762 Burning sensation
127027621 12702762 Diarrhoea
127027621 12702762 Dyspnoea
127027621 12702762 Gastrointestinal disorder
127027621 12702762 Insomnia
127027621 12702762 Intervertebral disc disorder
127027621 12702762 Nausea
127027621 12702762 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
127027621 12702762 1 20160610 20160615 0