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
124317205 12431720 5 F 20160902 20160603 20160905 EXP US-GILEAD-2016-0207831 GILEAD 73.00 YR E F Y 41.27000 KG 20160905 OT 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
124317205 12431720 1 PS AMBRISENTAN AMBRISENTAN 1 Unknown 5 MG, QD Y 1504767A 22081 5 MG TABLET QD
124317205 12431720 2 SS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD Y 1509507A 22081 10 MG TABLET QD
124317205 12431720 3 SS ADCIRCA TADALAFIL 1 Unknown UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124317205 12431720 1 Product used for unknown indication
124317205 12431720 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124317205 12431720 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124317205 12431720 Deafness
124317205 12431720 Ear congestion
124317205 12431720 Middle ear effusion
124317205 12431720 Musculoskeletal pain
124317205 12431720 Neck pain
124317205 12431720 Neuralgia
124317205 12431720 Pain

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

no results found

Therapies reported

no results found