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
116256603 11625660 3 F 20140212 20160907 20151013 20160923 EXP CA-GILEAD-2014-0095630 GILEAD 81.00 YR E F Y 0.00000 20160923 CN CA CA

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
116256603 11625660 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD D 22081 10 MG TABLET QD
116256603 11625660 2 SS ADCIRCA TADALAFIL 1 Unknown UNK U 0
116256603 11625660 3 C LASIX FUROSEMIDE 1 0
116256603 11625660 4 C CRESTOR ROSUVASTATIN CALCIUM 1 UNK U 0
116256603 11625660 5 C CRESTOR ROSUVASTATIN CALCIUM 1 UNK U 0
116256603 11625660 6 C METOPROLOL. METOPROLOL 1 U 0
116256603 11625660 7 C WARFARIN WARFARIN 1 U 0
116256603 11625660 8 C DIGOXIN. DIGOXIN 1 U 0
116256603 11625660 9 C CALCIUM CALCIUM 1 UNK U 0
116256603 11625660 10 C CALCIUM CALCIUM 1 UNK U 0
116256603 11625660 11 C CALCIUM CALCIUM 1 UNK U 0
116256603 11625660 12 C TOLOXIN /00017701/ 2 UNK U 0
116256603 11625660 13 C VITAMIN D CHOLECALCIFEROL 1 UNK U 0
116256603 11625660 14 C OXYGEN. OXYGEN 1 3 L, UNK U 0 3 L
116256603 11625660 15 C OXYGEN. OXYGEN 1 UNK U 0
116256603 11625660 16 C OXYGEN. OXYGEN 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116256603 11625660 1 Pulmonary arterial hypertension
116256603 11625660 2 Product used for unknown indication
116256603 11625660 3 Product used for unknown indication
116256603 11625660 4 Product used for unknown indication
116256603 11625660 6 Product used for unknown indication
116256603 11625660 7 Product used for unknown indication
116256603 11625660 8 Product used for unknown indication
116256603 11625660 9 Product used for unknown indication
116256603 11625660 12 Product used for unknown indication
116256603 11625660 13 Product used for unknown indication
116256603 11625660 14 Product used for unknown indication
116256603 11625660 15 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
116256603 11625660 DE
116256603 11625660 OT
116256603 11625660 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
116256603 11625660 Death
116256603 11625660 Diarrhoea
116256603 11625660 Dyspnoea
116256603 11625660 Faeces soft
116256603 11625660 Melaena
116256603 11625660 Oedema peripheral

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
116256603 11625660 1 20131107 0