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
101386365 10138636 5 F 20140414 20160615 20140429 20160630 EXP JP-FRI-1000066840 FOREST 84.84 YR M Y 49.00000 KG 20160630 OT FR JP

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
101386365 10138636 1 PS ACAMPROSATE ACAMPROSATE 1 Oral 1998 MG 21431 TABLET
101386365 10138636 2 SS CYANAMIDE CYANAMIDE 1 Oral 30 MG 0
101386365 10138636 3 C SERMION NICERGOLINE 1 0
101386365 10138636 4 C BLOPRESS CANDESARTAN CILEXETIL 1 0
101386365 10138636 5 C ADALAT NIFEDIPINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101386365 10138636 1 Alcoholism
101386365 10138636 2 Alcoholism
101386365 10138636 3 Product used for unknown indication
101386365 10138636 4 Product used for unknown indication
101386365 10138636 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
101386365 10138636 DE
101386365 10138636 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
101386365 10138636 Acute kidney injury
101386365 10138636 Subarachnoid haematoma
101386365 10138636 Subdural haematoma

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
101386365 10138636 1 20140303 20140317 0
101386365 10138636 2 20140317 20140331 0
101386365 10138636 3 20140303 20140414 0
101386365 10138636 4 20140303 20140414 0
101386365 10138636 5 20140303 20140414 0