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
126337961 12633796 1 I 20160616 20160803 20160809 20160809 EXP GB-MHRA-EYC 00143118 GB-PFIZER INC-2016373965 PFIZER 68.00 YR M Y 82.00000 KG 20160809 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
126337961 12633796 1 PS Atorvastatin ATORVASTATIN 1 Oral 10 MG, 1X/DAY 20 MG Y 20702 10 MG FILM-COATED TABLET QD
126337961 12633796 2 C INSULIN INSULIN NOS 1 UNK 0
126337961 12633796 3 C ATENOLOL. ATENOLOL 1 25 MG, UNK 0 25 MG
126337961 12633796 4 C DOXAZOSIN DOXAZOSINDOXAZOSIN MESYLATE 1 2 MG, UNK 0 2 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126337961 12633796 1 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
126337961 12633796 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126337961 12633796 Arthralgia
126337961 12633796 Joint lock
126337961 12633796 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
126337961 12633796 1 20160614 20160725 0