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
123729512 12372951 2 F 20160812 20160516 20160819 EXP GB-MYLANLABS-2016M1019306 MYLAN 0.00 Y 0.00000 20160819 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
123729512 12372951 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK U U UNKNOWN 75817
123729512 12372951 2 SS AMITRIPTYLIN AMITRIPTYLINE 1 UNK U U 0
123729512 12372951 3 SS PREGABALIN. PREGABALIN 1 600 MG, UNK U U 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123729512 12372951 1 Infection
123729512 12372951 2 Product used for unknown indication
123729512 12372951 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123729512 12372951 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123729512 12372951 Burning sensation
123729512 12372951 Depression
123729512 12372951 Feeling abnormal
123729512 12372951 Hypoaesthesia
123729512 12372951 Mental impairment
123729512 12372951 Musculoskeletal stiffness
123729512 12372951 Nerve injury
123729512 12372951 Neuropathy peripheral
123729512 12372951 Neurotoxicity
123729512 12372951 Pain
123729512 12372951 Pain in extremity
123729512 12372951 Paraesthesia
123729512 12372951 Tendon pain
123729512 12372951 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
123729512 12372951 1 201505 0