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
125298341 12529834 1 I 201606 0 20160705 20160705 DIR 51.00 YR F N 0.00000 20160701 N PH 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
125298341 12529834 1 PS SOMATULINE AUTOGEL LANREOTIDE ACETATE 1 Subcutaneous D D K18580 20170712 0 90 MG QM
125298341 12529834 3 C NORVASC AMLODIPINE BESYLATE 1 0
125298341 12529834 4 C LISINOPRIL. LISINOPRIL 1 0
125298341 12529834 6 C ZETIA EZETIMIBE 1 0
125298341 12529834 8 C MAGNESIUM MAGNESIUM 1 0
125298341 12529834 10 C TYLENOL ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125298341 12529834 1 Small intestine carcinoma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125298341 12529834 Diarrhoea
125298341 12529834 Headache

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

Event ID CASEID RPSR COD
125298341 12529834 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125298341 12529834 1 20160610 0