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
126273681 12627368 1 I 20151021 20160805 20160805 PER US-AMGEN-USASL2015111308 AMGEN 69.00 YR E M Y 0.00000 20160805 OT 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
126273681 12627368 1 PS NPLATE ROMIPLOSTIM 1 Unknown 750 MUG, Q3WK 125268 750 UG POWDER FOR INJECTION
126273681 12627368 2 SS NPLATE ROMIPLOSTIM 1 125268 POWDER FOR INJECTION
126273681 12627368 3 C ATIVAN LORAZEPAM 1 UNK 0
126273681 12627368 4 C VELCADE BORTEZOMIB 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126273681 12627368 1 Platelet count increased
126273681 12627368 2 Immune thrombocytopenic purpura

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126273681 12627368 Accidental overdose
126273681 12627368 Arthralgia
126273681 12627368 Dizziness
126273681 12627368 Fatigue
126273681 12627368 Inappropriate schedule of drug administration
126273681 12627368 Injection site bruising
126273681 12627368 Injection site pain
126273681 12627368 Laceration
126273681 12627368 Petechiae
126273681 12627368 Phantom pain
126273681 12627368 Platelet count abnormal
126273681 12627368 Respiratory tract congestion
126273681 12627368 Therapy non-responder
126273681 12627368 Wrong drug administered

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
126273681 12627368 1 20110101 0