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
127488081 12748808 1 I 20160830 20160909 20160915 20160915 EXP GB-ABBVIE-16P-167-1728994-00 ABBVIE 61.00 YR F Y 53.00000 KG 20160915 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
127488081 12748808 1 PS CLARITHROMYCIN. CLARITHROMYCIN 1 Oral 500 MG Y GG5020 50662
127488081 12748808 2 C OMEPRAZOLE. OMEPRAZOLE 1 0
127488081 12748808 3 C ATORVASTATIN ATORVASTATIN 1 0
127488081 12748808 4 C RAMIPRIL. RAMIPRIL 1 0
127488081 12748808 5 C ASPIRIN. ASPIRIN 1 0
127488081 12748808 6 C ATENOLOL. ATENOLOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127488081 12748808 1 Infection
127488081 12748808 2 Product used for unknown indication
127488081 12748808 3 Product used for unknown indication
127488081 12748808 4 Product used for unknown indication
127488081 12748808 5 Product used for unknown indication
127488081 12748808 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127488081 12748808 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127488081 12748808 Dizziness
127488081 12748808 Dysgeusia
127488081 12748808 Headache
127488081 12748808 Insomnia
127488081 12748808 Nausea
127488081 12748808 Pollakiuria

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
127488081 12748808 1 20160830 20160831 0