The Safety Rates Drug Report

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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
126397701 12639770 1 I 20160726 20160810 20160810 PER US-AMGEN-USASP2016098730 AMGEN 71.00 YR E F Y 0.00000 20160810 OT 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
126397701 12639770 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
126397701 12639770 2 SS ADALIMUMAB ADALIMUMAB 1 Unknown UNK 0
126397701 12639770 3 SS ROSUVASTATIN. ROSUVASTATIN 1 Unknown UNK 0
126397701 12639770 4 SS TAMOXIFEN TAMOXIFEN 1 Unknown UNK 0
126397701 12639770 5 C LIPITOR ATORVASTATIN CALCIUM 1 UNK 0
126397701 12639770 6 C LIPITOR ATORVASTATIN CALCIUM 1 Oral 40 MG, QD 0 40 MG QD
126397701 12639770 7 C LYRICA PREGABALIN 1 Oral 150 MG, BID 0 150 MG BID
126397701 12639770 8 C FOSAMAX ALENDRONATE SODIUM 1 Oral 7 MG, QWK 0 7 MG /wk
126397701 12639770 9 C ASPIRIN. ASPIRIN 1 81 MG, QD 0 81 MG QD
126397701 12639770 10 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 Oral Q6H, 5-325MG 0 QID
126397701 12639770 11 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 175 MUG, UNK 0 175 UG
126397701 12639770 12 C NALOXEGOL OXALATE. NALOXEGOL OXALATE 1 Oral 25 MG, QWK 0 25 MG /wk
126397701 12639770 13 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral 20 MG, QD 0 20 MG QD
126397701 12639770 14 C DITROPAN OXYBUTYNIN CHLORIDE 1 Oral 5 MG, BID 0 5 MG BID
126397701 12639770 15 C AZULFIDINE SULFASALAZINE 1 500 MG, UNK 0 500 MG
126397701 12639770 16 C IMITREX SUMATRIPTAN SUCCINATE 1 Subcutaneous 6 MG, BID 0 6 MG BID
126397701 12639770 17 C DESYREL TRAZODONE HYDROCHLORIDE 1 Oral 150 MG, BEDTIME 0 150 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126397701 12639770 1 Product used for unknown indication
126397701 12639770 2 Product used for unknown indication
126397701 12639770 3 Product used for unknown indication
126397701 12639770 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126397701 12639770 Drug hypersensitivity

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

no results found

Therapies reported

no results found