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
127432561 12743256 1 I 2006 20160908 20160914 20160914 EXP US-JNJFOC-20160909451 JANSSEN 0.00 A F Y 67.13000 KG 20160914 CN US 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
127432561 12743256 1 SS TRAMADOL HYDROCHLORIDE. TRAMADOL HYDROCHLORIDE 1 Oral 1 TABLET A DAY N 0 50 MG TABLETS QD
127432561 12743256 2 PS TRAMADOL HYDROCHLORIDE. TRAMADOL HYDROCHLORIDE 1 Oral N 20281 TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127432561 12743256 1 Pain
127432561 12743256 2 Pain

Outcome of event

Event ID CASEID OUTC COD
127432561 12743256 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127432561 12743256 Abnormal loss of weight
127432561 12743256 Anxiety
127432561 12743256 Back disorder
127432561 12743256 Blood pressure abnormal
127432561 12743256 Cholelithiasis
127432561 12743256 Diarrhoea
127432561 12743256 Joint injury
127432561 12743256 Therapeutic response unexpected

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
127432561 12743256 1 2006 0