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
127054861 12705486 1 I 20160809 0 20160831 20160831 DIR 69.02 YR F N 70.76000 KG 20160823 N MD 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
127054861 12705486 1 PS CARBOPLATIN. CARBOPLATIN 1 D D 0 989.5 MG
127054861 12705486 2 SS TAXOL PACLITAXEL 1 0 693 MG
127054861 12705486 4 C DEXAMETHASONE. DEXAMETHASONE 1 0
127054861 12705486 6 C FENTANYL. FENTANYL 1 0
127054861 12705486 8 C FUROSEMIDE. FUROSEMIDE 1 0
127054861 12705486 10 C NAPROXEN. NAPROXEN 1 0
127054861 12705486 12 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 0
127054861 12705486 14 C ONDANSETRON ONDANSETRON 1 0
127054861 12705486 16 C SENNA SENNA LEAFSENNOSIDESSENNOSIDES A AND B 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127054861 12705486 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127054861 12705486 Asthenia
127054861 12705486 Dehydration
127054861 12705486 Diarrhoea
127054861 12705486 Drug intolerance
127054861 12705486 Fatigue

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

Event ID CASEID RPSR COD
127054861 12705486 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127054861 12705486 1 20160729 0
127054861 12705486 2 20160729 0