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
126222561 12622256 1 I 20160716 20160726 20160804 20160804 EXP GB-MHRA-EYC 00142729 GB-PFIZER INC-2016362433 PFIZER 74.00 YR M Y 81.00000 KG 20160804 CN GB GB

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
126222561 12622256 1 PS ATORVASTATIN CALCIUM. ATORVASTATIN CALCIUM 1 20 MG, UNK N 02752 20702 20 MG
126222561 12622256 2 C RAMIPRIL. RAMIPRIL 1 UNK 0
126222561 12622256 3 C WARFARIN WARFARIN 1 UNK 0
126222561 12622256 4 C FINASTERIDE. FINASTERIDE 1 UNK 0
126222561 12622256 5 C ALFUZOSIN ALFUZOSIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126222561 12622256 1 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
126222561 12622256 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126222561 12622256 Cardiac fibrillation
126222561 12622256 Lymph node pain
126222561 12622256 Lymphadenopathy
126222561 12622256 Myalgia

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
126222561 12622256 1 20160714 20160717 0