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
126949221 12694922 1 I 20160817 20160829 20160829 EXP CA-PFIZER INC-2016406129 PFIZER 34.00 YR M Y 0.00000 20160829 OT CA CA

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
126949221 12694922 1 SS ENBREL ETANERCEPT 1 UNK U 0
126949221 12694922 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK U 11719
126949221 12694922 3 SS ARAVA LEFLUNOMIDE 1 UNK U 0 TABLET
126949221 12694922 4 SS HUMIRA ADALIMUMAB 1 UNK U 0
126949221 12694922 5 SS IMURAN AZATHIOPRINE 1 UNK U 0
126949221 12694922 6 SS NEORAL CYCLOSPORINE 1 Oral 200 MG, BID U 0 200 MG BID
126949221 12694922 7 SS REMICADE INFLIXIMAB 1 UNK U 0
126949221 12694922 8 SS STELARA USTEKINUMAB 1 UNK U 0
126949221 12694922 9 SS TOCILIZUMAB TOCILIZUMAB 1 UNK U 0
126949221 12694922 10 SS ULTRAVATE HALOBETASOL PROPIONATE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126949221 12694922 6 Psoriasis

Outcome of event

Event ID CASEID OUTC COD
126949221 12694922 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126949221 12694922 Drug eruption
126949221 12694922 Drug ineffective
126949221 12694922 Epistaxis
126949221 12694922 Hepatic function abnormal
126949221 12694922 Hypersensitivity
126949221 12694922 Muscle spasms
126949221 12694922 Pain in extremity
126949221 12694922 Pneumonia
126949221 12694922 Stomatitis
126949221 12694922 Urticaria

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

no results found

Therapies reported

no results found