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
65328013 6532801 3 F 2007 20160824 20080123 20160824 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-14046544 BRISTOL MYERS SQUIBB 38.84 YR F Y 0.00000 20160824 OT FR FR

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
65328013 6532801 1 PS SUSTIVA EFAVIRENZ 1 Oral UNK Y 20972 CAPSULE
65328013 6532801 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral UNK Y 0
65328013 6532801 3 SS COMBIVIR LAMIVUDINEIDOVUDINE 1 Oral UNK 0
65328013 6532801 4 SS KALETRA LOPINAVIRRITONAVIR 1 Oral UNK 0
65328013 6532801 5 SS DEPAMIDE VALPROMIDE 1 Oral 1200 MG, QD Y 0 1200 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
65328013 6532801 1 Antiretroviral therapy
65328013 6532801 2 Antiretroviral therapy
65328013 6532801 3 Antiretroviral therapy
65328013 6532801 4 Antiretroviral therapy
65328013 6532801 5 Bipolar disorder

Outcome of event

Event ID CASEID OUTC COD
65328013 6532801 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
65328013 6532801 Caesarean section
65328013 6532801 HELLP syndrome
65328013 6532801 Mania
65328013 6532801 Maternal exposure during pregnancy
65328013 6532801 Pre-eclampsia
65328013 6532801 Premature delivery
65328013 6532801 Twin 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
65328013 6532801 1 20070328 20070808 0
65328013 6532801 2 20070328 20070808 0
65328013 6532801 3 20070808 0
65328013 6532801 4 20070808 0
65328013 6532801 5 20061001 20070804 0