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
98856872 9885687 2 F 201306 20160713 20140210 20160722 EXP BR-PFIZER INC-2014033897 PFIZER 42.00 YR F Y 60.00000 KG 20160722 CN BR BR

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
98856872 9885687 1 PS LYRICA PREGABALIN 1 75 MG, 1X/DAY 21446 75 MG CAPSULE, HARD QD
98856872 9885687 2 SS LYRICA PREGABALIN 1 Oral 150 MG, 1X/DAY (2 TABLETS OF 75 MG PER DAY OR 1 TABLET OF 150 MG DAILY) 21446 150 MG CAPSULE, HARD QD
98856872 9885687 3 SS LYRICA PREGABALIN 1 75 MG, 1X/DAY 21446 75 MG CAPSULE, HARD QD
98856872 9885687 4 C MIRTAX /00428402/ 2 Oral 1 TABLET AT NIGHT 0 1 DF TABLET QD
98856872 9885687 5 C ALPRAZOLAM. ALPRAZOLAM 1 Oral 1 TABLET OF 1 MG AT NIGHT 0 1 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98856872 9885687 1 Pain
98856872 9885687 2 Arthritis
98856872 9885687 4 Arthritis
98856872 9885687 5 Anxiety

Outcome of event

Event ID CASEID OUTC COD
98856872 9885687 HO
98856872 9885687 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
98856872 9885687 Dizziness
98856872 9885687 Dysstasia
98856872 9885687 Nausea
98856872 9885687 Pain
98856872 9885687 Pleural effusion
98856872 9885687 Pneumonia
98856872 9885687 Tendonitis

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
98856872 9885687 1 2012 0
98856872 9885687 2 201603 0
98856872 9885687 4 201603 201605 0
98856872 9885687 5 2013 0