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
123881032 12388103 2 F 20160812 20160520 20160826 EXP GB-LUPIN PHARMACEUTICALS INC.-E2B_00005432 LUPIN 0.00 F Y 0.00000 20160826 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
123881032 12388103 1 SS Amitriptyline AMITRIPTYLINE 1 Unknown U UNKNOWN 0
123881032 12388103 2 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown U UNKNOWN 200563
123881032 12388103 3 SS PREGABALIN. PREGABALIN 1 Unknown U UNKNOWN 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123881032 12388103 1 Product used for unknown indication
123881032 12388103 2 Infection
123881032 12388103 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123881032 12388103 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123881032 12388103 Burning sensation
123881032 12388103 Depression
123881032 12388103 Feeling abnormal
123881032 12388103 Hypoaesthesia
123881032 12388103 Mental impairment
123881032 12388103 Musculoskeletal stiffness
123881032 12388103 Nerve injury
123881032 12388103 Neuropathy peripheral
123881032 12388103 Neurotoxicity
123881032 12388103 Pain
123881032 12388103 Pain in extremity
123881032 12388103 Paraesthesia
123881032 12388103 Tendon pain
123881032 12388103 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
123881032 12388103 2 201505 0