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
103695953 10369595 3 F 20160210 20140807 20160922 PER US-AMGEN INC.-USASP2014021123 AMGEN 56.00 YR A F Y 0.00000 20160922 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
103695953 10369595 1 PS NEUPOGEN FILGRASTIM 1 Subcutaneous 480 MUG, UNK U 103353 480 UG UNKNOWN FORMULATION
103695953 10369595 2 SS HERCEPTIN TRASTUZUMAB 1 Intravenous (not otherwise specified) 270 MG, UNK 0 270 MG SOLUTION FOR INFUSION
103695953 10369595 3 SS HERCEPTIN TRASTUZUMAB 1 Intravenous (not otherwise specified) 135 MG, UNK 0 135 MG SOLUTION FOR INFUSION
103695953 10369595 4 SS BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown UNK 0
103695953 10369595 5 C ATIVAN LORAZEPAM 1 0.5 MG, UNK 0 .5 MG
103695953 10369595 6 C ALOXI PALONOSETRON HYDROCHLORIDE 1 0.75 MG, UNK 0 .75 MG
103695953 10369595 7 C COMPAZINE PROCHLORPERAZINE MALEATE 1 Oral 10 MG, UNK 0 10 MG
103695953 10369595 8 C TAXOTERE DOCETAXEL 1 130 MG, UNK 0 130 MG
103695953 10369595 9 C EMEND APREPITANT 1 150 MG, UNK 0 150 MG
103695953 10369595 10 C NEULASTA PEGFILGRASTIM 1 Intravenous (not otherwise specified) UNK 0 UNKNOWN FORMULATION
103695953 10369595 11 C ZOFRAN ONDANSETRON HYDROCHLORIDE 1 Intravenous (not otherwise specified) UNK 0
103695953 10369595 12 C DEXAMETHASONE. DEXAMETHASONE 1 20 MG, UNK 0 20 MG
103695953 10369595 13 C CARBOPLATIN. CARBOPLATIN 1 600 MG, UNK 0 600 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103695953 10369595 1 Breast cancer
103695953 10369595 2 Breast cancer
103695953 10369595 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
103695953 10369595 Abdominal pain
103695953 10369595 Drug hypersensitivity
103695953 10369595 Eye disorder
103695953 10369595 Fatigue
103695953 10369595 Local swelling

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
103695953 10369595 1 20110729 20110729 0
103695953 10369595 2 20110715 20110715 0
103695953 10369595 3 20110722 20110722 0
103695953 10369595 5 20110715 20110715 0
103695953 10369595 6 20110715 20110715 0
103695953 10369595 7 20110722 20110722 0
103695953 10369595 8 20110715 20110715 0
103695953 10369595 9 20110715 20110715 0
103695953 10369595 10 20110919 20110919 0
103695953 10369595 11 20110919 20110919 0
103695953 10369595 12 20110715 20110715 0
103695953 10369595 13 20110715 20110715 0