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
123653692 12365369 2 F 20160812 20160513 20160819 EXP GB-PFIZER INC-2016248831 PFIZER 0.00 F 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
123653692 12365369 1 PS PREGABALIN. PREGABALIN 1 600 MG, UNK U 21446 600 MG
123653692 12365369 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK U UNKNOWN 77245
123653692 12365369 3 SS AMITRIPTYLIN AMITRIPTYLINE 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
123653692 12365369 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123653692 12365369 Anxiety
123653692 12365369 Burning sensation
123653692 12365369 Depression
123653692 12365369 Feeling abnormal
123653692 12365369 Hypoaesthesia
123653692 12365369 Mental impairment
123653692 12365369 Musculoskeletal stiffness
123653692 12365369 Nerve injury
123653692 12365369 Neuropathy peripheral
123653692 12365369 Neurotoxicity
123653692 12365369 Pain
123653692 12365369 Pain in extremity
123653692 12365369 Paraesthesia
123653692 12365369 Tendon pain
123653692 12365369 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
123653692 12365369 2 201505 0