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
91575604 9157560 4 F 20160916 20130312 20160921 EXP US-RB-050760-13 INDIVIOR 0.00 Y 0.00000 20160921 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
91575604 9157560 1 PS SUBUTEX BUPRENORPHINE HYDROCHLORIDE 1 Unknown UNK U UNKNOWN 20732 SUBLINGUAL TABLET
91575604 9157560 2 SS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Unknown UNK U U UNKNOWN 0 SUBLINGUAL TABLET
91575604 9157560 3 SS Buprenorphine/Naloxone generic BUPRENORPHINENALOXONE 1 Unknown UNK U U UNKNOWN 0 SUBLINGUAL TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
91575604 9157560 1 Pain
91575604 9157560 2 Pain
91575604 9157560 3 Pain

Outcome of event

Event ID CASEID OUTC COD
91575604 9157560 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
91575604 9157560 Anxiety
91575604 9157560 Asthenia
91575604 9157560 Back pain
91575604 9157560 Diarrhoea
91575604 9157560 Drug withdrawal syndrome
91575604 9157560 Feeling abnormal
91575604 9157560 Haematemesis
91575604 9157560 Insomnia
91575604 9157560 Off label use
91575604 9157560 Restless legs syndrome
91575604 9157560 Substance abuse
91575604 9157560 Tremor
91575604 9157560 Vomiting

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

no results found

Therapies reported

no results found