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
123915002 12391500 2 F 20160812 20160521 20160824 EXP GB-MHRA-ADR 23466161 GB-ACCORD-040684 ACCORD 0.00 F Y 0.00000 20160824 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
123915002 12391500 1 PS AMITRIPTYLINE AMITRIPTYLINE 1 U 202446
123915002 12391500 2 SS CIPROFLOXACIN/CIPROFLOXACIN HYDROCHLORIDE/CIPROFLOXACIN LACTATE CIPROFLOXACIN 1 U UNKNOWN 200750048
123915002 12391500 3 SS PREGABALIN. PREGABALIN 1 U 4024 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123915002 12391500 1 Product used for unknown indication
123915002 12391500 2 Infection
123915002 12391500 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123915002 12391500 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123915002 12391500 Anxiety
123915002 12391500 Depression
123915002 12391500 Feeling abnormal
123915002 12391500 Mental impairment
123915002 12391500 Musculoskeletal stiffness
123915002 12391500 Nerve injury
123915002 12391500 Neuropathy peripheral
123915002 12391500 Neurotoxicity
123915002 12391500 Pain in extremity
123915002 12391500 Tendon pain
123915002 12391500 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
123915002 12391500 2 201505 0