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
104520704 10452070 4 F 20160725 20140915 20160725 EXP CH-JNJFOC-20140908436 JANSSEN 75.00 YR E F Y 0.00000 20160725 CN CH CH

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
104520704 10452070 1 PS IBUPROFEN. IBUPROFEN 1 Unknown U U 17463 UNSPECIFIED
104520704 10452070 2 SS PARACETAMOL ACETAMINOPHEN 1 U U 19872 UNSPECIFIED
104520704 10452070 3 SS PARACETAMOL ACETAMINOPHEN 1 U U 19872 UNSPECIFIED
104520704 10452070 4 SS TRAMADOL HCL TRAMADOL HYDROCHLORIDE 1 Unknown U U UNKNOWN 21692 UNSPECIFIED
104520704 10452070 5 SS DICLOFENAC DICLOFENAC 1 Unknown U U 999999 UNSPECIFIED
104520704 10452070 6 SS STEROIDS NOS UNSPECIFIED INGREDIENT 1 Intravenous (not otherwise specified) U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104520704 10452070 1 Back pain
104520704 10452070 3 Back pain
104520704 10452070 4 Back pain
104520704 10452070 5 Back pain
104520704 10452070 6 Back pain

Outcome of event

Event ID CASEID OUTC COD
104520704 10452070 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
104520704 10452070 Decreased appetite
104520704 10452070 Drug ineffective
104520704 10452070 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found