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
127479531 12747953 1 I 201605 20160908 20160915 20160915 EXP US-ABBVIE-16P-163-1722942-00 ABBVIE 90.00 YR F Y 0.00000 20160915 CN 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
127479531 12747953 1 PS TRICOR FENOFIBRATE 1 Unknown UNKNOWN 19304
127479531 12747953 2 SS VASCEPA ICOSAPENT ETHYL 1 Unknown U 0
127479531 12747953 3 C PROBIOTIC PROBIOTICS NOS 1 Unknown 0
127479531 12747953 4 C CALCIUM CALCIUM 1 Unknown 0
127479531 12747953 5 C VITAMIN D CHOLECALCIFEROL 1 Unknown 0
127479531 12747953 6 C MULTIVITAMIN VITAMINS 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127479531 12747953 1 Product used for unknown indication
127479531 12747953 2 Product used for unknown indication
127479531 12747953 3 Product used for unknown indication
127479531 12747953 4 Product used for unknown indication
127479531 12747953 5 Product used for unknown indication
127479531 12747953 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127479531 12747953 HO
127479531 12747953 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127479531 12747953 Blood pressure decreased
127479531 12747953 Cardiac failure
127479531 12747953 Fall
127479531 12747953 Fatigue
127479531 12747953 Pulmonary embolism
127479531 12747953 Upper limb fracture

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

no results found

Therapies reported

no results found