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
125819981 12581998 1 I 2001 20160523 20160722 20160722 EXP US-STRIDES ARCOLAB LIMITED-2016SP003780 STRIDES 0.00 Y 0.00000 20160722 OT US 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
125819981 12581998 1 PS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 500 MG, QD 90055 500 MG
125819981 12581998 2 SS PREDNISOLONE. PREDNISOLONE 1 7.5 MG, QD 0 7.5 MG
125819981 12581998 3 SS PREDNISOLONE. PREDNISOLONE 1 5 MG, UNK 0 5 MG
125819981 12581998 4 SS CYCLOSPORIN A CYCLOSPORINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125819981 12581998 1 Immunosuppression
125819981 12581998 2 Immunosuppression
125819981 12581998 4 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
125819981 12581998 HO
125819981 12581998 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125819981 12581998 Abdominal pain
125819981 12581998 Asthenia
125819981 12581998 Blood creatinine increased
125819981 12581998 Clostridium difficile colitis
125819981 12581998 Cytomegalovirus infection
125819981 12581998 Diarrhoea haemorrhagic
125819981 12581998 Herpes zoster
125819981 12581998 Intestinal haemorrhage
125819981 12581998 Neutropenia
125819981 12581998 Pneumonia
125819981 12581998 Pseudomonas infection
125819981 12581998 Pyrexia
125819981 12581998 Sepsis
125819981 12581998 Thrombocytopenia
125819981 12581998 Urinary tract infection

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

no results found

Therapies reported

no results found