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
125893261 12589326 1 I 20160430 20160630 20160725 20160725 PER US-JNJFOC-20160702076 JANSSEN 44.24 YR A F Y 0.00000 20160725 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
125893261 12589326 1 PS MOTRIN IBUPROFEN 1 Unknown N N UNK 19012 UNSPECIFIED
125893261 12589326 2 SS MOTRIN IBUPROFEN 1 Unknown N N UNK 19012 UNSPECIFIED
125893261 12589326 3 C JANUVIA SITAGLIPTIN PHOSPHATE 1 Unknown 0 UNSPECIFIED
125893261 12589326 4 C FOLIC ACID. FOLIC ACID 1 Unknown 0 UNSPECIFIED
125893261 12589326 5 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown 0 UNSPECIFIED
125893261 12589326 6 C METHOTREXATE. METHOTREXATE 1 Unknown 0 UNSPECIFIED
125893261 12589326 7 C REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) 0 300 MG LYOPHILIZED POWDER QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125893261 12589326 2 Headache
125893261 12589326 3 Diabetes mellitus
125893261 12589326 4 Rheumatoid arthritis
125893261 12589326 5 Rheumatoid arthritis
125893261 12589326 6 Rheumatoid arthritis
125893261 12589326 7 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125893261 12589326 Drug ineffective
125893261 12589326 Vomiting

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
125893261 12589326 2 20160430 0
125893261 12589326 7 20160427 20160511 0