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
107229762 10722976 2 F 20160324 20150120 20160331 EXP PHEH2015US001049 NOVARTIS 0.00 F Y 0.00000 20160401 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
107229762 10722976 1 PS LESCOL XL FLUVASTATIN SODIUM 1 Unknown 21192 SLOW RELEASE TABLET
107229762 10722976 2 SS LIPITOR ATORVASTATIN CALCIUM 1 Unknown 0
107229762 10722976 3 C MULTI VITAMIN VITAMINS 1 Unknown UNK 0
107229762 10722976 4 C GILOTRIF AFATINIB 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107229762 10722976 1 Product used for unknown indication
107229762 10722976 2 Product used for unknown indication
107229762 10722976 3 Product used for unknown indication
107229762 10722976 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
107229762 10722976 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
107229762 10722976 Eye disorder
107229762 10722976 Femur fracture
107229762 10722976 Nail bed infection
107229762 10722976 Neoplasm malignant
107229762 10722976 Pain

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

no results found

Therapies reported

no results found