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
126241501 12624150 1 I 20160427 20160802 20160805 20160805 EXP FR-ROCHE-1808044 ROCHE 49.00 YR F Y 51.00000 KG 20160805 MD FR FR

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
126241501 12624150 1 PS MABTHERA RITUXIMAB 1 Unknown DAY 1?ON DAY 14 10/MAY/2016, DRUG WAS DISCONTINUED Y 103705 1 G
126241501 12624150 2 SS CORTANCYL PREDNISONE 1 Oral U 0 20 MG QD
126241501 12624150 3 SS HYDROCORTISONE. HYDROCORTISONE 1 Oral U 0 15 MG QD
126241501 12624150 4 SS OROCAL D3 CALCIUM CARBONATECHOLECALCIFEROL 1 Oral U 0 1 DF BID
126241501 12624150 5 SS ACTONEL RISEDRONATE SODIUM 1 Oral U 0 35 MG /wk
126241501 12624150 6 SS DIFFU K POTASSIUM CHLORIDE 1 Oral U 0 600 MG QD
126241501 12624150 7 SS PARACETAMOL ACETAMINOPHEN 1 Oral U 0 1 DF QID
126241501 12624150 8 SS TRAMADOL. TRAMADOL 1 Oral U 0 50 MG QD
126241501 12624150 9 SS ZAMUDOL TRAMADOL HYDROCHLORIDE 1 Oral U 0 100 MG BID
126241501 12624150 10 SS ADCIRCA TADALAFIL 1 Oral Y 0 20 MG BID
126241501 12624150 11 SS IMOVANE ZOPICLONE 1 Oral U 0 1 DF QD
126241501 12624150 12 SS NEFOPAM NEFOPAM 1 Sublingual U 0 20 MG TID
126241501 12624150 13 SS ALPRAZOLAM. ALPRAZOLAM 1 Oral 1 DF = 0.25 MG U 0 .5 DF TID
126241501 12624150 14 SS COUMADINE WARFARIN SODIUM 1 Oral U 0 8 MG QD
126241501 12624150 15 SS INNOHEP TINZAPARIN SODIUM 1 Subcutaneous U 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126241501 12624150 1 Product used for unknown indication
126241501 12624150 2 Product used for unknown indication
126241501 12624150 3 Product used for unknown indication
126241501 12624150 4 Product used for unknown indication
126241501 12624150 5 Product used for unknown indication
126241501 12624150 6 Product used for unknown indication
126241501 12624150 7 Product used for unknown indication
126241501 12624150 8 Product used for unknown indication
126241501 12624150 9 Product used for unknown indication
126241501 12624150 10 Product used for unknown indication
126241501 12624150 11 Product used for unknown indication
126241501 12624150 12 Product used for unknown indication
126241501 12624150 13 Product used for unknown indication
126241501 12624150 14 Product used for unknown indication
126241501 12624150 15 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126241501 12624150 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126241501 12624150 Hypotension
126241501 12624150 Rash macular
126241501 12624150 Urticaria

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
126241501 12624150 1 20160427 0
126241501 12624150 2 20160317 0
126241501 12624150 3 20160317 0
126241501 12624150 4 20160316 0
126241501 12624150 5 20160316 0
126241501 12624150 6 20160317 0
126241501 12624150 7 20160317 0
126241501 12624150 8 20160419 0
126241501 12624150 9 20160425 0
126241501 12624150 10 20160422 20160427 0
126241501 12624150 11 20160422 0
126241501 12624150 12 20160418 0
126241501 12624150 13 20160423 0
126241501 12624150 14 20160316 20160319 0
126241501 12624150 15 20160318 0