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
125362431 12536243 1 I 20160613 20160701 20160707 20160707 EXP GB-MHRA-TPP7837931C90713YC1466522470797 GB-GALDERMA-GB16004556 GALDERMA 74.00 YR M Y 70.00000 KG 20160707 OT 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
125362431 12536243 1 PS DOXYCYCLINE. DOXYCYCLINE 1 U 50783
125362431 12536243 2 C AMLODIPINE AMLODIPINE BESYLATE 1 0 1 DF QD
125362431 12536243 3 C ASPIRIN. ASPIRIN 1 0 1 DF QD
125362431 12536243 4 C LEVOTHYROXINE. LEVOTHYROXINE 1 0 1 DF QD
125362431 12536243 5 C OMEPRAZOLE. OMEPRAZOLE 1 0 1 DF QD
125362431 12536243 6 C PARACETAMOL ACETAMINOPHEN 1 0 2 DF QID
125362431 12536243 7 C TETRACYCLINE TETRACYCLINE 1 0 1 DF QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125362431 12536243 1 Product used for unknown indication
125362431 12536243 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125362431 12536243 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125362431 12536243 Abdominal pain
125362431 12536243 Malaise

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
125362431 12536243 1 20160613 0
125362431 12536243 2 20160114 0
125362431 12536243 3 20150615 0
125362431 12536243 4 20150615 0
125362431 12536243 5 20150615 0
125362431 12536243 6 20150615 0
125362431 12536243 7 20160621 0