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
125976753 12597675 3 F 2015 20160831 20160727 20160912 EXP IT-MINISAL02-368202 IT-MYLANLABS-2016M1030521 MYLAN 0.00 Y 0.00000 20160912 MD IT IT

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
125976753 12597675 1 PS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) 60 MG/M2, CYCLE U 91540 60 MG/M**2 CONCENTRATE FOR SOLUTION FOR INFUSION
125976753 12597675 2 SS HERCEPTIN TRASTUZUMAB 1 Intravenous (not otherwise specified) 6 ?G/KG, CYCLE U 0 6 UG/KG
125976753 12597675 3 C MICARDIS TELMISARTAN 1 UNK 0
125976753 12597675 4 C RYTMONORM PROPAFENONE 1 UNK 0
125976753 12597675 5 C PARIET RABEPRAZOLE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125976753 12597675 1 Breast cancer
125976753 12597675 2 Breast cancer
125976753 12597675 3 Hypertension
125976753 12597675 4 Hypertension
125976753 12597675 5 Gastritis

Outcome of event

Event ID CASEID OUTC COD
125976753 12597675 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125976753 12597675 Thrombocytopenia

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
125976753 12597675 1 20150720 0
125976753 12597675 2 20130730 20160810 0