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
127022901 12702290 1 I 201608 20160823 20160831 20160831 EXP US-AMGEN-USASL2016111172 AMGEN 60.00 YR A F Y 0.00000 20160831 MD 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
127022901 12702290 1 PS NPLATE ROMIPLOSTIM 1 Unknown 200 UNITS OF NPLATE EACH DOSE U 125268 POWDER FOR INJECTION
127022901 12702290 2 SS PROLIA DENOSUMAB 1 Unknown UNK UNK, Q6MO U 0 SOLUTION FOR INJECTION
127022901 12702290 3 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Unknown 0
127022901 12702290 4 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown 0
127022901 12702290 5 C IMURAN AZATHIOPRINE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127022901 12702290 1 Immune thrombocytopenic purpura
127022901 12702290 2 Osteoporosis postmenopausal
127022901 12702290 3 Allergy to animal

Outcome of event

Event ID CASEID OUTC COD
127022901 12702290 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127022901 12702290 Contusion
127022901 12702290 Infusion site bruising
127022901 12702290 Platelet count decreased
127022901 12702290 Systemic lupus erythematosus

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
127022901 12702290 1 201502 0