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
127273801 12727380 1 I 20160829 20160909 20160909 EXP NO-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-123673 RANBAXY 54.00 YR F Y 0.00000 20160909 OT NO NO

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
127273801 12727380 1 PS CARBOPLATIN. CARBOPLATIN 1 Unknown UNK U 77926
127273801 12727380 2 SS NAVELBINE VINORELBINE TARTRATE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127273801 12727380 1 Product used for unknown indication
127273801 12727380 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127273801 12727380 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127273801 12727380 Anaemia
127273801 12727380 Fatigue
127273801 12727380 Neutrophil count decreased
127273801 12727380 Pneumonia
127273801 12727380 Pyrexia
127273801 12727380 Weight decreased

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

no results found

Therapies reported

no results found