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
123914442 12391444 2 F 20160812 20160520 20160826 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-116980 RANBAXY 0.00 F Y 0.00000 20160826 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
123914442 12391444 1 PS Amitriptyline AMITRIPTYLINE 1 Unknown UNK U U 40816
123914442 12391444 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown UNK U U UNKNOWN 0
123914442 12391444 3 SS PREGABALIN. PREGABALIN 1 Unknown 600 MG, UNK U U 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123914442 12391444 1 Product used for unknown indication
123914442 12391444 2 Infection
123914442 12391444 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123914442 12391444 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123914442 12391444 Burning sensation
123914442 12391444 Depression
123914442 12391444 Feeling abnormal
123914442 12391444 Hypoaesthesia
123914442 12391444 Mental impairment
123914442 12391444 Musculoskeletal stiffness
123914442 12391444 Nerve injury
123914442 12391444 Neuropathy peripheral
123914442 12391444 Neurotoxicity
123914442 12391444 Pain
123914442 12391444 Pain in extremity
123914442 12391444 Paraesthesia
123914442 12391444 Tendon pain
123914442 12391444 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
123914442 12391444 2 201505 0