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
127261191 12726119 1 I 20160827 20160908 20160908 EXP CA-JNJFOC-20160826382 JANSSEN 0.00 A Y 0.00000 20160908 MD CA CA

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
127261191 12726119 1 PS STELARA USTEKINUMAB 1 Subcutaneous U U 125261 SOLUTION FOR INJECTION
127261191 12726119 2 SS STELARA USTEKINUMAB 1 Intravenous (not otherwise specified) U U 125261 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127261191 12726119 1 Crohn's disease
127261191 12726119 2 Crohn's disease

Outcome of event

Event ID CASEID OUTC COD
127261191 12726119 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127261191 12726119 Alopecia
127261191 12726119 Arthralgia
127261191 12726119 Clostridium difficile infection
127261191 12726119 Headache
127261191 12726119 Infection
127261191 12726119 Injection related reaction
127261191 12726119 Rash
127261191 12726119 Respiratory tract infection
127261191 12726119 Skin infection
127261191 12726119 Soft tissue infection

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

no results found

Therapies reported

no results found