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
126560101 12656010 1 I 20160520 20160816 20160816 PER US-ROCHE-1761918 ROCHE 0.00 F Y 0.00000 20160816 CN 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
126560101 12656010 1 PS PEGASYS PEGINTERFERON ALFA-2A 1 Subcutaneous B3025B10 103964 180 MG /wk
126560101 12656010 2 C CEPHALEXIN. CEPHALEXIN 1 Unknown 0 500 MG CAPSULE
126560101 12656010 3 C LABETALOL LABETALOLLABETALOL HYDROCHLORIDE 1 Unknown 0 100 MG TABLET
126560101 12656010 4 C PHENTERMINE. PHENTERMINE 1 Unknown 0 37.5 MG TABLET
126560101 12656010 5 C IBUPROFEN. IBUPROFEN 1 Unknown 0 600 MG TABLET
126560101 12656010 6 C ATORVASTATIN ATORVASTATIN 1 Unknown 0 10 MG TABLET
126560101 12656010 7 C METRONIDAZOL METRONIDAZOLE 1 Unknown 0 500 MG TABLET
126560101 12656010 8 C ENOXAPARIN ENOXAPARIN 1 Unknown 40/0.4 ML 0
126560101 12656010 9 C PROGESTERONE. PROGESTERONE 1 Unknown 0 200 MG CAPSULE
126560101 12656010 10 C LOVENOX ENOXAPARIN SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126560101 12656010 1 Thrombolysis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126560101 12656010 No adverse event
126560101 12656010 Pregnancy

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
126560101 12656010 1 20160311 201604 0