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
126532501 12653250 1 I 20160616 20160803 20160815 20160815 EXP GB-MHRA-EYC 00143118 GB-TEVA-683078ACC TEVA 68.00 YR M Y 82.00000 KG 20160816 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
126532501 12653250 1 PS ATORVASTATIN ATORVASTATIN 1 Oral 10 MILLIGRAM DAILY; 20 MG Y U 78773 10 MG QD
126532501 12653250 2 C INSULIN INSULIN NOS 1 0
126532501 12653250 3 C ATENOLOL. ATENOLOL 1 0 25 MG
126532501 12653250 4 C DOXAZOSIN DOXAZOSINDOXAZOSIN MESYLATE 1 0 2 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126532501 12653250 1 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
126532501 12653250 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126532501 12653250 Arthralgia
126532501 12653250 Joint lock
126532501 12653250 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
126532501 12653250 1 20160614 20160725 0