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
98868867 9886886 7 F 20121026 20160902 20140210 20160929 EXP UG-BRISTOL-MYERS SQUIBB COMPANY-17227166 BRISTOL MYERS SQUIBB 34.20 YR F Y 39.00000 KG 20160929 CN US UG

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
98868867 9886886 1 SS ETOPOSIDE. ETOPOSIDE 1 Oral 50 MG, QD Y 0 50 MG QD
98868867 9886886 2 PS EFAVIRENZ, EMTRICITABINE, AND TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1100 MG, QD 21937 1100 MG FILM-COATED TABLET QD
98868867 9886886 3 SS EXTERNAL-ISONIAZID ISONIAZID 1 Oral UNK U 0 QD
98868867 9886886 4 C ETHAMBUTOL ETHAMBUTOL HYDROCHLORIDE 1 Oral UNK UNK, QD U 0 QD
98868867 9886886 5 C RIFAMPICIN RIFAMPIN 1 Oral UNK, QD U 0 QD
98868867 9886886 6 C PYRAZINAMIDE. PYRAZINAMIDE 1 Oral UNK UNK, QD U 0 QD
98868867 9886886 7 C PYRIDOXINE PYRIDOXINE 1 Oral LAST DOSE: 10DEC12 U 0 QD
98868867 9886886 8 C TRAMADOL. TRAMADOL 1 Oral LAST DOSE: 04DEC12 U 0
98868867 9886886 9 C COTRIMOXAZOLE SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral UNK U 0
98868867 9886886 10 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 Intravenous (not otherwise specified) UNK, BID U 0 BID
98868867 9886886 11 C POTASSIUM CHLORIDE. POTASSIUM CHLORIDE 1 Intravenous drip UNK U 0 INJECTION
98868867 9886886 12 C SALINE /00075401/ SODIUM CHLORIDE 1 Intravenous drip UNK, Q6H U 0 INFUSION QID
98868867 9886886 13 C VINCRISTINE VINCRISTINE 1 Intravenous (not otherwise specified) UNK U 0
98868867 9886886 14 C BLEOMYCIN BLEOMYCIN SULFATE 1 Intravenous (not otherwise specified) UNK U 0
98868867 9886886 15 C DEXAMETHASONE. DEXAMETHASONE 1 Intravenous (not otherwise specified) UNK U 0
98868867 9886886 16 C CEFTRIAXONE. CEFTRIAXONE 1 Intravenous (not otherwise specified) UNK, QD U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98868867 9886886 1 HIV infection
98868867 9886886 2 HIV infection
98868867 9886886 3 Tuberculosis
98868867 9886886 4 Tuberculosis
98868867 9886886 5 Tuberculosis
98868867 9886886 6 Tuberculosis
98868867 9886886 7 Neuropathy peripheral
98868867 9886886 8 Pain
98868867 9886886 9 Prophylaxis
98868867 9886886 10 Vomiting
98868867 9886886 11 Hypokalaemia
98868867 9886886 12 Hyponatraemia
98868867 9886886 13 Chemotherapy
98868867 9886886 14 Chemotherapy
98868867 9886886 15 Product used for unknown indication
98868867 9886886 16 Bacterial infection

Outcome of event

Event ID CASEID OUTC COD
98868867 9886886 OT
98868867 9886886 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
98868867 9886886 Burning sensation
98868867 9886886 Diarrhoea
98868867 9886886 Hypokalaemia
98868867 9886886 Hyponatraemia
98868867 9886886 Malaise
98868867 9886886 Muscular weakness
98868867 9886886 Neuropathy peripheral
98868867 9886886 Neutropenia
98868867 9886886 Pyrexia
98868867 9886886 Vomiting

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
98868867 9886886 1 20121115 0
98868867 9886886 2 20121114 0
98868867 9886886 13 20130703 20131107 0
98868867 9886886 14 20130703 20131107 0