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
124713184 12471318 4 F 20160419 20160829 20160616 20160906 EXP US-PFIZER INC-2016286630 PFIZER 74.00 YR F Y 88.00000 KG 20160906 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
124713184 12471318 1 PS LEVOXYL LEVOTHYROXINE SODIUM 1 Oral 50 UG, 1X/DAY 21301 50 UG TABLET QD
124713184 12471318 2 C ASPIRIN. ASPIRIN 1 Oral 81 MG, DAILY 0 81 MG TABLET
124713184 12471318 3 C CLARITIN LORATADINE 1 Oral 10 MG, DAILY 0 10 MG TABLET
124713184 12471318 4 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 40 MG, DAILY 0 40 MG
124713184 12471318 5 C VITAMIN D3 CHOLECALCIFEROL 1 Oral 5000 IU, DAILY 0 5000 IU
124713184 12471318 6 C VITAMIN E .ALPHA.-TOCOPHEROL 1 Oral 400 IU, DAILY 0 400 IU

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124713184 12471318 1 Hypothyroidism
124713184 12471318 4 Hiatus hernia

Outcome of event

Event ID CASEID OUTC COD
124713184 12471318 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124713184 12471318 Cataract
124713184 12471318 Disturbance in attention
124713184 12471318 Fatigue
124713184 12471318 Insomnia
124713184 12471318 Lactose intolerance
124713184 12471318 Somnolence

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found