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
123875022 12387502 2 F 20160812 20160520 20160826 EXP GB-AUROBINDO-AUR-APL-2016-05950 AUROBINDO 0.00 F Y 0.00000 20160826 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
123875022 12387502 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown UNK U U UNKNOWN 77859
123875022 12387502 2 SS PREGABALIN. PREGABALIN 1 Unknown 600 MG, UNK U U 0 600 MG
123875022 12387502 3 SS AMITRIPTYLIN AMITRIPTYLINE 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123875022 12387502 1 Infection
123875022 12387502 2 Product used for unknown indication
123875022 12387502 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123875022 12387502 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123875022 12387502 Burning sensation
123875022 12387502 Depression
123875022 12387502 Feeling abnormal
123875022 12387502 Hypoaesthesia
123875022 12387502 Mental impairment
123875022 12387502 Musculoskeletal stiffness
123875022 12387502 Nerve injury
123875022 12387502 Neuropathy peripheral
123875022 12387502 Neurotoxicity
123875022 12387502 Pain
123875022 12387502 Pain in extremity
123875022 12387502 Paraesthesia
123875022 12387502 Tendon pain
123875022 12387502 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
123875022 12387502 1 201505 0