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
123699252 12369925 2 F 20160812 20160516 20160825 EXP GB-TEVA-659158ACC TEVA 0.00 F Y 0.00000 20160825 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
123699252 12369925 1 SS AMITRIPTYLIN AMITRIPTYLINE 1 U U 0
123699252 12369925 2 PS CIPROFLOXACIN. CIPROFLOXACIN 1 U U UNKNOWN 74124
123699252 12369925 3 SS PREGABALIN. PREGABALIN 1 U U 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123699252 12369925 1 Product used for unknown indication
123699252 12369925 2 Infection
123699252 12369925 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123699252 12369925 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123699252 12369925 Burning sensation
123699252 12369925 Depression
123699252 12369925 Feeling abnormal
123699252 12369925 Hypoaesthesia
123699252 12369925 Mental impairment
123699252 12369925 Musculoskeletal stiffness
123699252 12369925 Nerve injury
123699252 12369925 Neuropathy peripheral
123699252 12369925 Neurotoxicity
123699252 12369925 Pain
123699252 12369925 Pain in extremity
123699252 12369925 Paraesthesia
123699252 12369925 Tendon pain
123699252 12369925 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
123699252 12369925 2 201505 0