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
93227817 9322781 7 F 201212 20160721 20130601 20160725 EXP CA-ROCHE-1230056 ROCHE 66.74 YR F Y 59.00000 KG 20160725 MD 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
93227817 9322781 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 400 MG SOLUTION FOR INFUSION
93227817 9322781 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 392 MG SOLUTION FOR INFUSION
93227817 9322781 3 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 386.4 MG SOLUTION FOR INFUSION
93227817 9322781 4 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 408 MG SOLUTION FOR INFUSION
93227817 9322781 5 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 417.6 MG SOLUTION FOR INFUSION
93227817 9322781 6 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 406 MG SOLUTION FOR INFUSION
93227817 9322781 7 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 418 MG SOLUTION FOR INFUSION
93227817 9322781 8 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 442 MG SOLUTION FOR INFUSION
93227817 9322781 9 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 436 MG SOLUTION FOR INFUSION
93227817 9322781 10 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 440 MG SOLUTION FOR INFUSION
93227817 9322781 11 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 458.4 MG SOLUTION FOR INFUSION
93227817 9322781 12 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 468 MG SOLUTION FOR INFUSION
93227817 9322781 13 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 442 MG SOLUTION FOR INFUSION
93227817 9322781 14 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 472 MG SOLUTION FOR INFUSION
93227817 9322781 15 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 492 MG SOLUTION FOR INFUSION Q3W
93227817 9322781 16 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 493.6 MG SOLUTION FOR INFUSION Q3W
93227817 9322781 17 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 496.6 MG SOLUTION FOR INFUSION Q3W
93227817 9322781 18 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 492 MG SOLUTION FOR INFUSION
93227817 9322781 19 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 472 MG SOLUTION FOR INFUSION
93227817 9322781 20 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 488.8 MG SOLUTION FOR INFUSION
93227817 9322781 21 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 489 MG SOLUTION FOR INFUSION
93227817 9322781 22 SS RIVOTRIL CLONAZEPAM 1 Unknown U 17533
93227817 9322781 23 C PROZAC FLUOXETINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 0
93227817 9322781 24 C CARDIZEM DILTIAZEM HYDROCHLORIDE 1 0
93227817 9322781 25 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 0
93227817 9322781 26 C PREMARIN ESTROGENS, CONJUGATED 1 0
93227817 9322781 27 C ZANTAC RANITIDINE HYDROCHLORIDE 1 0
93227817 9322781 28 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 0
93227817 9322781 29 C MORPHINE MORPHINE 1 0
93227817 9322781 30 C STATEX (CANADA) MORPHINE SULFATE 1 0
93227817 9322781 31 C IMOVANE ZOPICLONE 1 0
93227817 9322781 32 C TYLENOL ACETAMINOPHEN 1 0
93227817 9322781 33 C GRAVOL DIMENHYDRINATE 1 0
93227817 9322781 34 C METHOTREXATE. METHOTREXATE 1 0
93227817 9322781 35 C FOLIC ACID. FOLIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93227817 9322781 1 Rheumatoid arthritis
93227817 9322781 22 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
93227817 9322781 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
93227817 9322781 Bronchitis
93227817 9322781 Cardiac failure
93227817 9322781 Cystitis
93227817 9322781 Dizziness
93227817 9322781 Drug effect decreased
93227817 9322781 Emphysema
93227817 9322781 Fall
93227817 9322781 General physical health deterioration
93227817 9322781 Nausea
93227817 9322781 Weight increased

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
93227817 9322781 1 20101229 0
93227817 9322781 2 20110203 0
93227817 9322781 3 20110307 0
93227817 9322781 4 20110419 0
93227817 9322781 5 20110517 0
93227817 9322781 6 20110719 0
93227817 9322781 7 20110831 0
93227817 9322781 8 20110928 0
93227817 9322781 9 20111019 0
93227817 9322781 10 20111123 0
93227817 9322781 11 20120104 0
93227817 9322781 12 20120201 0
93227817 9322781 13 20120411 0
93227817 9322781 14 20120601 0
93227817 9322781 15 20120629 0
93227817 9322781 16 20120810 0
93227817 9322781 17 20120927 0
93227817 9322781 18 20121116 0
93227817 9322781 19 20130125 0
93227817 9322781 20 20130222 0
93227817 9322781 21 20130606 20131108 0