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
125895652 12589565 2 F 20160720 20160725 20160727 EXP US-GILEAD-2016-0215311 GILEAD 68.00 YR E F Y 0.00000 20160727 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
125895652 12589565 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD 1504768A 22081 10 MG TABLET QD
125895652 12589565 2 SS ADCIRCA TADALAFIL 1 Unknown 20 MG, BID N 0 20 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125895652 12589565 1 Product used for unknown indication
125895652 12589565 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125895652 12589565 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125895652 12589565 Bone pain
125895652 12589565 Chest discomfort
125895652 12589565 Chills
125895652 12589565 Condition aggravated
125895652 12589565 Cough
125895652 12589565 Dyspnoea
125895652 12589565 Eye swelling
125895652 12589565 Headache
125895652 12589565 Lung disorder
125895652 12589565 Pain in extremity
125895652 12589565 Peripheral swelling
125895652 12589565 Rheumatoid arthritis
125895652 12589565 Tremor
125895652 12589565 Upper-airway cough syndrome

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
125895652 12589565 1 201605 0
125895652 12589565 2 201605 0