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
97384397 9738439 7 F 201210 20150929 20131208 20151001 EXP CA-ROCHE-1148266 ROCHE 76.81 YR M Y 100.00000 KG 20151001 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
97384397 9738439 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) U 125276 788 MG
97384397 9738439 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) U 125276 800 MG
97384397 9738439 3 C METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown 0 500 MG QID
97384397 9738439 4 C ALLOPURINOL. ALLOPURINOL 1 Unknown 0 300 MG
97384397 9738439 5 C LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 Unknown 0 .15 MG
97384397 9738439 6 C FERROUS GLUCONATE FERROUS GLUCONATE 1 0
97384397 9738439 7 C SIMVASTATIN. SIMVASTATIN 1 0
97384397 9738439 8 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 0
97384397 9738439 9 C ATIVAN LORAZEPAM 1 0
97384397 9738439 10 C JANUVIA SITAGLIPTIN PHOSPHATE 1 Unknown 0 100 MG
97384397 9738439 11 C GLICLAZIDE GLICLAZIDE 1 Unknown 0 30 MG BID
97384397 9738439 12 C TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 0
97384397 9738439 13 C ASA ASPIRIN 1 0
97384397 9738439 14 C SOTALOL. SOTALOL 1 Unknown HALF A TABLET TWICE DAILY 0 80 MG
97384397 9738439 15 C TECTA PANTOPRAZOLE MAGNESIUM 1 Unknown 0 40 MG
97384397 9738439 16 C CANDESARTAN CANDESARTAN 1 Unknown 0 16 MG
97384397 9738439 17 C PREDNISONE. PREDNISONE 1 Unknown 0 3 MG
97384397 9738439 18 C METHOTREXATE METHOTREXATE 1 0
97384397 9738439 19 C ACTONEL RISEDRONATE SODIUM 1 0
97384397 9738439 20 C PLAVIX CLOPIDOGREL BISULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97384397 9738439 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
97384397 9738439 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97384397 9738439 Aphasia
97384397 9738439 Cerebrovascular accident
97384397 9738439 Device malfunction
97384397 9738439 Diverticulitis
97384397 9738439 Drug ineffective
97384397 9738439 Fatigue
97384397 9738439 Fungal infection
97384397 9738439 Headache
97384397 9738439 Heart rate decreased
97384397 9738439 Heart rate increased
97384397 9738439 Musculoskeletal pain
97384397 9738439 Myalgia
97384397 9738439 Nasopharyngitis
97384397 9738439 Pain
97384397 9738439 Peripheral swelling
97384397 9738439 Rash
97384397 9738439 Squamous cell carcinoma of skin
97384397 9738439 Swelling
97384397 9738439 Tenderness
97384397 9738439 Thermal burn
97384397 9738439 Visual impairment
97384397 9738439 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
97384397 9738439 1 20120228 20150820 0
97384397 9738439 2 20130117 0