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
116381114 11638111 4 F 2014 20160902 20151016 20160912 EXP CR-ABBVIE-15K-039-1483100-00 ABBVIE 56.44 YR F Y 80.00000 KG 20160912 CN COUNTRY NOT SPECIFIED CR

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
116381114 11638111 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
116381114 11638111 2 SS TRAMAL TRAMADOL 1 Unknown U UNKNOWN 0
116381114 11638111 3 SS TRAMAL TRAMADOL 1 Unknown U UNKNOWN 0 TID
116381114 11638111 4 SS NOLVADEX TAMOXIFEN CITRATE 1 Unknown U UNKNOWN 0
116381114 11638111 5 C ACETAMINOPHEN. ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116381114 11638111 1 Rheumatoid arthritis
116381114 11638111 2 Pain
116381114 11638111 4 Product used for unknown indication
116381114 11638111 5 Pain

Outcome of event

Event ID CASEID OUTC COD
116381114 11638111 OT
116381114 11638111 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
116381114 11638111 Bone pain
116381114 11638111 Depressed mood
116381114 11638111 Dizziness
116381114 11638111 Fibrosis
116381114 11638111 Intraductal proliferative breast lesion
116381114 11638111 Malaise
116381114 11638111 Nerve compression
116381114 11638111 Postoperative wound complication
116381114 11638111 Radicular pain
116381114 11638111 Somnolence
116381114 11638111 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
116381114 11638111 1 20120820 0