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
127991361 12799136 1 I 20160706 20160707 20160930 20160930 EXP JP-009507513-1607JPN004266 MERCK 68.00 YR M Y 68.00000 KG 20160930 PH JP 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
127991361 12799136 1 PS TEMODAL TEMOZOLOMIDE 1 Oral TOTAL DAILY DOSE 120 MG, DIVIDED DOSE FREQUENCY UNKNOWN 7440 MG Y 21029 120 MG CAPSULE QD
127991361 12799136 2 SS TEMODAL TEMOZOLOMIDE 1 Oral TOTAL DAILY DOSE 260 MG, DIVIDED DOSE FREQUENCY UNKNOWN 7440 MG Y 21029 260 MG CAPSULE QD
127991361 12799136 3 SS FAMOTIDINE. FAMOTIDINE 1 Oral DAILY DOSAGE UNKNOWN U 0 TABLET
127991361 12799136 4 SS CORTRIL HYDROCORTISONE 1 Unknown DAILY DOSAGE UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127991361 12799136 1 Neoplasm progression

Outcome of event

Event ID CASEID OUTC COD
127991361 12799136 OT
127991361 12799136 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127991361 12799136 Eczema
127991361 12799136 Pancytopenia
127991361 12799136 Rash
127991361 12799136 Vomiting

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
127991361 12799136 1 20160408 20160608 0
127991361 12799136 2 20160706 20160707 0