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
127562281 12756228 1 I 20160317 20160918 20160918 EXP US-TEVA-2016-06269 TEVA 72.00 YR F Y 0.00000 20160918 CN COUNTRY NOT SPECIFIED 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
127562281 12756228 1 PS NABUMETONE. NABUMETONE 1 Oral 750 MG, BID Y UNKNOWN 91083 750 MG BID
127562281 12756228 2 SS NABUMETONE. NABUMETONE 1 Oral 750 MG, DAILY Y UNKNOWN 91083 750 MG QD
127562281 12756228 3 C TOPAMAX TOPIRAMATE 1 Oral UNK, UNKNOWN UNKNOWN 0
127562281 12756228 4 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Oral UNK, UNKNOWN UNKNOWN 0
127562281 12756228 5 C PRAVASTATIN. PRAVASTATIN 1 Oral UNK, UNKNOWN UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127562281 12756228 1 Osteoarthritis
127562281 12756228 2 Pain
127562281 12756228 3 Pain
127562281 12756228 4 Hypertension
127562281 12756228 5 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
127562281 12756228 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127562281 12756228 Asthenia
127562281 12756228 Dizziness
127562281 12756228 Epistaxis
127562281 12756228 Haemorrhage
127562281 12756228 Thrombosis

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

no results found

Therapies reported

no results found