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
123464092 12346409 2 F 20160719 20160509 20160728 EXP GB-DRREDDYS-GER/UKI/16/0079406 DR REDDYS 0.00 F Y 0.00000 20160728 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
123464092 12346409 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 U U UNKNOWN 75593
123464092 12346409 2 SS PREGABALIN. PREGABALIN 1 U U 0 600 MG
123464092 12346409 3 SS Amitriptylin AMITRIPTYLINE 1 U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123464092 12346409 1 Infection
123464092 12346409 2 Product used for unknown indication
123464092 12346409 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123464092 12346409 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123464092 12346409 Burning sensation
123464092 12346409 Depression
123464092 12346409 Feeling abnormal
123464092 12346409 Hypoaesthesia
123464092 12346409 Mental impairment
123464092 12346409 Musculoskeletal stiffness
123464092 12346409 Nerve injury
123464092 12346409 Neuropathy peripheral
123464092 12346409 Neurotoxicity
123464092 12346409 Pain
123464092 12346409 Pain in extremity
123464092 12346409 Paraesthesia
123464092 12346409 Tendon pain
123464092 12346409 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
123464092 12346409 1 201505 0