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
127021401 12702140 1 I 201608 20160823 20160831 20160831 EXP US-AMGEN-USASP2016111415 AMGEN 0.00 F Y 0.00000 20160831 PH 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
127021401 12702140 1 PS NEULASTA PEGFILGRASTIM 1 Unknown UNK U 125031 SOLUTION FOR INJECTION
127021401 12702140 2 C CYTOXAN CYCLOPHOSPHAMIDE 1 UNK, Q2WK 0 QOW
127021401 12702140 3 C DOXORUBICIN DOXORUBICIN 1 UNK, Q2WK 0 QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127021401 12702140 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127021401 12702140 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127021401 12702140 Arthralgia
127021401 12702140 Feeling abnormal
127021401 12702140 Haemoglobin abnormal
127021401 12702140 Joint swelling
127021401 12702140 Leukocyte vacuolisation
127021401 12702140 Muscle spasms
127021401 12702140 Neutrophil count increased
127021401 12702140 Neutrophil toxic granulation present
127021401 12702140 Urinary tract infection
127021401 12702140 White blood cell count increased
127021401 12702140 White blood cell morphology abnormal

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

no results found

Therapies reported

no results found