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
121761092 12176109 2 F 20160115 20160721 20160314 20160727 EXP CHPA2016US003042 GLAXOSMITHKLINE 0.00 Y 0.00000 20160727 CN US US

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
121761092 12176109 1 SS Acetylsalicylic acid ASPIRIN 1 Oral 81 MG, QD UNKNOWN 0 81 MG QD
121761092 12176109 2 PS VOLTAREN DICLOFENAC SODIUM 1 UNK UNK 22122 GEL

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121761092 12176109 1 Product used for unknown indication
121761092 12176109 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121761092 12176109 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121761092 12176109 Accident
121761092 12176109 Arthritis
121761092 12176109 Chondrocalcinosis pyrophosphate
121761092 12176109 Gastrointestinal haemorrhage
121761092 12176109 Swelling
121761092 12176109 Upper limb fracture
121761092 12176109 Wrong technique in product usage process

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
121761092 12176109 1 2003 0