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
126782901 12678290 1 I 20160809 20160823 20160823 EXP GB-TEVA-684554ACC TEVA 46.00 YR F Y 0.00000 20160823 CN GB GB

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
126782901 12678290 1 PS PROPRANOLOL PROPRANOLOLPROPRANOLOL HYDROCHLORIDE 1 Unknown U U UNKNOWN 70233 40 MG TABLET
126782901 12678290 2 SS SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown U U UNKNOWN 40353 100 MG TABLET
126782901 12678290 3 SS COTRIMOXAZOLE SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown U U UNKNOWN 0 TABLET
126782901 12678290 4 SS DARUNAVIR DARUNAVIR 1 Oral U U UNKNOWN 0 800 MG TABLET
126782901 12678290 5 SS EMTRICITABINE AND TENOFOVIR EMTRICITABINETENOFOVIR 1 Unknown U U UNKNOWN 0 TABLET
126782901 12678290 6 SS NORVIR RITONAVIR 1 Unknown U U UNKNOWN 0 100 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126782901 12678290 1 Product used for unknown indication
126782901 12678290 2 Product used for unknown indication
126782901 12678290 3 Product used for unknown indication
126782901 12678290 4 HIV infection
126782901 12678290 5 HIV infection
126782901 12678290 6 HIV infection

Outcome of event

Event ID CASEID OUTC COD
126782901 12678290 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126782901 12678290 Cerebrovascular accident

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

no results found

Therapies reported

no results found