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
102522562 10252256 2 F 201104 20160627 20140623 20160705 EXP US-ROCHE-1418176 ROCHE 68.24 YR F Y 0.00000 20160705 MD 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
102522562 10252256 1 PS CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Oral 500MG QD X 3 DAYS, 500MG BID X 3 WEEK, 1000MG BID U 50723 500 MG TABLET QD
102522562 10252256 2 SS FLOLAN EPOPROSTENOL SODIUM 1 Unknown 28 NG/KG/MIN M362 0
102522562 10252256 3 SS FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 28 NG/KG/MIN M362 0 INFUSION
102522562 10252256 4 SS FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 28 NG/KG/MIN M362 0 INFUSION
102522562 10252256 5 SS FLOLAN EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) 28 NG/KG/MIN M362 0
102522562 10252256 6 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown U 0 200 MG TABLET QD
102522562 10252256 7 C LASIX FUROSEMIDE 1 0
102522562 10252256 8 C CLARITIN LORATADINE 1 0
102522562 10252256 9 C OCUVITE PRESERVISION 2 0
102522562 10252256 10 C POTASSIUM CHLORIDE. POTASSIUM CHLORIDE 1 0
102522562 10252256 11 C ADCIRCA TADALAFIL 1 0
102522562 10252256 12 C TRACLEER BOSENTAN 1 0
102522562 10252256 13 C EPOPROSTENOL SODIUM. EPOPROSTENOL SODIUM 1 0
102522562 10252256 14 C ASPIRIN. ASPIRIN 1 0
102522562 10252256 15 C FLUTICASONE PROPIONATE. FLUTICASONE PROPIONATE 1 0
102522562 10252256 16 C TRAMADOL HCL TRAMADOL HYDROCHLORIDE 1 0
102522562 10252256 17 C TRIAMCINOLONE ACETONIDE. TRIAMCINOLONE ACETONIDE 1 0
102522562 10252256 18 C ZOLPIDEM TARTRATE. ZOLPIDEM TARTRATE 1 0
102522562 10252256 19 C PREDNISONE. PREDNISONE 1 0
102522562 10252256 20 C IMURAN AZATHIOPRINE 1 0
102522562 10252256 21 C BABY ASPIRIN ASPIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102522562 10252256 1 Arthralgia
102522562 10252256 2 Cor pulmonale chronic
102522562 10252256 3 Pulmonary hypertension
102522562 10252256 4 Polymyositis
102522562 10252256 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
102522562 10252256 HO
102522562 10252256 LT
102522562 10252256 OT
102522562 10252256 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
102522562 10252256 Asthenia
102522562 10252256 Blood bilirubin increased
102522562 10252256 Catheter site discharge
102522562 10252256 Catheterisation cardiac
102522562 10252256 Complication associated with device
102522562 10252256 Death
102522562 10252256 Diarrhoea
102522562 10252256 Dizziness
102522562 10252256 Ear infection
102522562 10252256 Ejection fraction decreased
102522562 10252256 Flushing
102522562 10252256 Herpes zoster
102522562 10252256 Hypertension
102522562 10252256 Hypoaesthesia
102522562 10252256 Left ventricular dysfunction
102522562 10252256 Liver function test increased
102522562 10252256 Loss of consciousness
102522562 10252256 Oedema peripheral
102522562 10252256 Right ventricular heave
102522562 10252256 Syncope
102522562 10252256 Tachycardia
102522562 10252256 Upper respiratory tract infection

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
102522562 10252256 2 20100525 0
102522562 10252256 3 20120201 0
102522562 10252256 4 20110314 0
102522562 10252256 5 20100222 0