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
125902182 12590218 2 F 201606 20160722 20160725 20160729 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-47193BP BOEHRINGER INGELHEIM 83.21 YR F Y 0.00000 20160729 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
125902182 12590218 1 PS AGGRENOX ASPIRINDIPYRIDAMOLE 1 Oral 2 ANZ Y 20884 CAPSULE BID
125902182 12590218 2 C CELEBREX CELECOXIB 1 Unknown 0
125902182 12590218 3 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown 0
125902182 12590218 4 C MICARDIS TELMISARTAN 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125902182 12590218 1 Transient ischaemic attack
125902182 12590218 2 Arthritis
125902182 12590218 3 Gastrooesophageal reflux disease
125902182 12590218 4 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125902182 12590218 OT
125902182 12590218 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125902182 12590218 Asthenia
125902182 12590218 Cerebrovascular accident
125902182 12590218 Gait disturbance
125902182 12590218 Pulmonary embolism
125902182 12590218 Transient ischaemic attack
125902182 12590218 Urinary tract infection

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
125902182 12590218 1 2011 20160706 0