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
123720792 12372079 2 F 20160812 20160516 20160823 EXP ALCN2016GB003192 ALCON 0.00 F Y 0.00000 20160823 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
123720792 12372079 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown UNK U 20369
123720792 12372079 2 SS AMITRIPTYLINE AMITRIPTYLINE 1 Unknown UNK U 0
123720792 12372079 3 SS PREGABALIN. PREGABALIN 1 Unknown 600 MG, UNK U 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123720792 12372079 1 Infection
123720792 12372079 2 Product used for unknown indication
123720792 12372079 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123720792 12372079 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123720792 12372079 Burning sensation
123720792 12372079 Depression
123720792 12372079 Feeling abnormal
123720792 12372079 Hypoaesthesia
123720792 12372079 Mental impairment
123720792 12372079 Musculoskeletal stiffness
123720792 12372079 Nerve injury
123720792 12372079 Neuropathy peripheral
123720792 12372079 Neurotoxicity
123720792 12372079 Pain
123720792 12372079 Pain in extremity
123720792 12372079 Paraesthesia
123720792 12372079 Tendon pain
123720792 12372079 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
123720792 12372079 1 201505 0