The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5378178 6329400 I 5378178-5 20070530 20070627 20070705 EXP US-JNJFOC-20070600960 JOHNSON + JOHNSON PHARMACEUTICAL R+D F Y 79.83 KG 20070705 MD UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5378178 1008662146 PS PREZISTA 1 ORAL 00108 21976
5378178 1008662147 SS PREZISTA 1 ORAL 00108 062477
5378178 1008662148 SS RITONAVIR 2 UNKNOWN 40195;40196
5378178 1008662149 SS ETRAVIRINE 1 ORAL 20127
5378178 1008662150 C TRUVADA 1 UNKNOWN 100067
5378178 1008662151 C REYATAZ 1 UNKNOWN
5378178 1008662152 C ATRIPLA 1 ORAL
5378178 1008662153 C IBUPROFEN 1 ORAL
5378178 1008662154 C KEFLEX 1 ORAL
5378178 1008662155 C ULTRAM 1 ORAL
5378178 1008662156 C LORTAB 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
5378178 1008662147 HIV INFECTION
5378178 1008662148 HIV INFECTION
5378178 1008662149 HIV INFECTION
5378178 1008662150 HIV INFECTION
5378178 1008662151 HIV INFECTION
5378178 1008662152 HIV INFECTION

Outcome of event

Event ID OUTC COD
5378178 OT

Reactions reported

Event ID PT
5378178 ASPARTATE AMINOTRANSFERASE INCREASED

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

no results found

Therapies reported

no results found