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
125419261 12541926 1 I 20160613 20160630 20160708 20160708 EXP GB-MHRA-TPP7837931C90713YC1466522470797 GB-MYLANLABS-2016M1027970 MYLAN 0.00 Y 0.00000 20160708 MD 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
125419261 12541926 1 PS DOXYCYCLINE. DOXYCYCLINE 1 UNK U U 62337
125419261 12541926 2 C AMLODIPINE AMLODIPINE BESYLATE 1 1 DF, QD 150.957993 DF U 0 1 DF QD
125419261 12541926 3 C ASPIRIN /00002701/ ASPIRIN 1 1 DF, QD 364 DF U 0 1 DF QD
125419261 12541926 4 C LEVOTHYROXINE. LEVOTHYROXINE 1 EACH MORNING 364 DF U 0 1 DF QD
125419261 12541926 5 C OMEPRAZOLE. OMEPRAZOLE 1 1 DF, QD 364 DF U 0 1 DF QD
125419261 12541926 6 C PARACETAMOL ACETAMINOPHEN 1 2 DF, QID 2912 DF U 0 2 DF QID
125419261 12541926 7 C TETRACYCLINE TETRACYCLINE 1 1 DF, QID 32 DF U 0 1 DF QID

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125419261 12541926 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125419261 12541926 Abdominal pain
125419261 12541926 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
125419261 12541926 1 20160613 0
125419261 12541926 2 20160114 0
125419261 12541926 3 20150615 0
125419261 12541926 4 20150615 0
125419261 12541926 5 20150615 0
125419261 12541926 6 20150615 0
125419261 12541926 7 20160621 0