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
127200341 12720034 1 I 20160823 20160907 20160907 EXP US-MLMSERVICE-20160818-0397617-1 US-ALKEM LABORATORIES LIMITED-US-ALKEM-2016-00159 ALKEM 10.00 YR M Y 0.00000 20160907 CN GB 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
127200341 12720034 1 PS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 UNKNOWN 91249
127200341 12720034 2 SS CICLOSPORIN CYCLOSPORINE 1 UNKNOWN 0
127200341 12720034 3 C TREOSULFAN TREOSULFAN 1 UNKNOWN 0
127200341 12720034 4 C FLUDARABINE FLUDARABINE PHOSPHATE 1 UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127200341 12720034 1 Prophylaxis against graft versus host disease
127200341 12720034 2 Prophylaxis against graft versus host disease
127200341 12720034 3 Product used for unknown indication
127200341 12720034 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127200341 12720034 OT
127200341 12720034 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127200341 12720034 Cardiac failure
127200341 12720034 Cardiac failure acute
127200341 12720034 Cough
127200341 12720034 Disease progression
127200341 12720034 Lower respiratory tract infection
127200341 12720034 Multiple organ dysfunction syndrome
127200341 12720034 Nasal congestion
127200341 12720034 Pulmonary oedema
127200341 12720034 Respiratory distress
127200341 12720034 Upper respiratory tract infection

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

no results found

Therapies reported

no results found