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
126506181 12650618 1 I 1991 20160810 20160815 20160815 EXP FR-ROCHE-1812585 ROCHE 45.00 YR F Y 0.00000 20160815 MD FR FR

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
126506181 12650618 1 PS RIVOTRIL CLONAZEPAM 1 Oral 2.5 MG/ML U 17533
126506181 12650618 2 SS MORPHINE MORPHINE 1 Subcutaneous 15 TO 20 MG U 0
126506181 12650618 3 C CODEINE CODEINE 1 0
126506181 12650618 4 C DUROGESIC FENTANYL 1 0
126506181 12650618 5 C ZAMUDOL TRAMADOL HYDROCHLORIDE 1 Unknown 1 DOSE IN THE MORNING AND 1 DOSE IN THE EVENING 0 150 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126506181 12650618 1 Product used for unknown indication
126506181 12650618 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126506181 12650618 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126506181 12650618 Anxiety
126506181 12650618 Drug dependence
126506181 12650618 Insomnia

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
126506181 12650618 1 2006 0
126506181 12650618 2 1985 0