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
126180021 12618002 1 I 20080414 20100804 20160803 20160803 EXP GB-ASTELLAS-2010003214 ASTELLAS 82.06 YR M Y 0.00000 20160803 CN 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
126180021 12618002 1 PS PLACEBO UNSPECIFIED INGREDIENT 1 Oral UNK UNK, ONCE DAILY 0 FORMULATION UNKNOWN QD
126180021 12618002 2 C TRAMADOL. TRAMADOL 1 Oral U 0 100 MG FORMULATION UNKNOWN
126180021 12618002 3 C PARACETAMOL ACETAMINOPHEN 1 Oral U 0 1 G FORMULATION UNKNOWN
126180021 12618002 4 C Tamsulosin TAMSULOSIN 1 Oral U 0 4000 MG FORMULATION UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126180021 12618002 1 Non-small cell lung cancer
126180021 12618002 2 Product used for unknown indication
126180021 12618002 3 Product used for unknown indication
126180021 12618002 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126180021 12618002 DE
126180021 12618002 HO
126180021 12618002 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126180021 12618002 Hypercalcaemia
126180021 12618002 Malignant neoplasm progression

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
126180021 12618002 1 20080222 200805 0
126180021 12618002 2 20080511 0
126180021 12618002 3 20080511 0
126180021 12618002 4 20080511 0