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
123759312 12375931 2 F 20160812 20160517 20160824 EXP GB-BAYER-2016-087506 BAYER 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
123759312 12375931 1 PS CIPROFLOXACIN MONOHYDROCHLORIDE CIPROFLOXACIN 1 UNK U 19537
123759312 12375931 2 SS AMITRIPTYLINE AMITRIPTYLINE 1 UNK U 0
123759312 12375931 3 SS PREGABALIN. PREGABALIN 1 600 MG, UNK 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123759312 12375931 1 Infection
123759312 12375931 2 Product used for unknown indication
123759312 12375931 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123759312 12375931 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123759312 12375931 Burning sensation
123759312 12375931 Depression
123759312 12375931 Feeling abnormal
123759312 12375931 Hypoaesthesia
123759312 12375931 Mental impairment
123759312 12375931 Musculoskeletal stiffness
123759312 12375931 Nerve injury
123759312 12375931 Neuropathy peripheral
123759312 12375931 Neurotoxicity
123759312 12375931 Pain
123759312 12375931 Pain in extremity
123759312 12375931 Paraesthesia
123759312 12375931 Tendon pain
123759312 12375931 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
123759312 12375931 1 201505 0