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
119139216 11913921 6 F 20160712 20160113 20160715 EXP US-GILEAD-2016-0191853 GILEAD 58.00 YR A F Y 0.00000 20160715 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
119139216 11913921 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 5 MG, QD NZYD 22081 5 MG TABLET QD
119139216 11913921 2 SS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD 1504768A 22081 10 MG TABLET QD
119139216 11913921 3 SS ADCIRCA TADALAFIL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119139216 11913921 1 Product used for unknown indication
119139216 11913921 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119139216 11913921 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119139216 11913921 Chest pain
119139216 11913921 Diarrhoea
119139216 11913921 Dysentery
119139216 11913921 Dyspnoea
119139216 11913921 Dyspnoea at rest
119139216 11913921 Dyspnoea exertional
119139216 11913921 Eye swelling
119139216 11913921 Headache
119139216 11913921 Insomnia
119139216 11913921 Nasopharyngitis
119139216 11913921 Neoplasm malignant
119139216 11913921 Peripheral swelling
119139216 11913921 Systemic lupus erythematosus
119139216 11913921 Unevaluable event
119139216 11913921 Weight decreased

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
119139216 11913921 1 20151208 0
119139216 11913921 2 20151208 0