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
126261141 12626114 1 I 20160705 20160802 20160805 20160805 EXP FR-JNJFOC-20160802186 JANSSEN 54.61 YR A F Y 0.00000 20160805 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
126261141 12626114 1 PS HALDOL HALOPERIDOL 1 Oral N N 15923 UNSPECIFIED
126261141 12626114 2 SS PAROXETINE. PAROXETINE 1 Oral N 0 UNKNOWN
126261141 12626114 3 SS KEPPRA LEVETIRACETAM 1 Oral 1.5 TABLET IN THE MORNING AND IN THE EVENING N 0 1.5 DF COATED TABLET BID
126261141 12626114 4 SS GARDENAL PHENOBARBITAL 1 Oral N 0 UNKNOWN
126261141 12626114 5 SS DIHYDAN PHENYTOIN 1 Oral IN THE MORNING AND IN THE EVENING N 0 100 MG TABLET BID
126261141 12626114 6 SS URBANYL CLOBAZAM 1 Oral N 0 10 MG UNKNOWN TID
126261141 12626114 7 SS STILNOX ZOLPIDEM TARTRATE 1 Oral IN THE EVENING N 0 10 MG COATED TABLET QD
126261141 12626114 8 C DIFFU K POTASSIUM CHLORIDE 1 Unknown 0 1 DF CAPSULE TID
126261141 12626114 9 C FOSAVANCE ALENDRONATE SODIUMCHOLECALCIFEROL 1 Unknown 0 70 MG UNKNOWN
126261141 12626114 10 C AMLOR AMLODIPINE BESYLATE 1 Unknown 0 10 MG UNKNOWN
126261141 12626114 11 C LOPERAMIDE LOPERAMIDE 1 Unknown 0 UNKNOWN
126261141 12626114 12 C LEVOTHYROX LEVOTHYROXINE 1 Unknown IN THE MORNING 0 50 UG UNKNOWN QD
126261141 12626114 13 C VESICARE SOLIFENACIN SUCCINATE 1 Unknown IN THE MORNING 0 10 MG UNKNOWN QD
126261141 12626114 14 C INEXIUM ESOMEPRAZOLE 1 Unknown 0 40 MG UNKNOWN QD
126261141 12626114 15 C METOJECT METHOTREXATE SODIUM 1 Unknown 0 1 DF INJECTION
126261141 12626114 16 C LOVENOX ENOXAPARIN SODIUM 1 Unknown 0 .6 ML UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126261141 12626114 1 Product used for unknown indication
126261141 12626114 2 Product used for unknown indication
126261141 12626114 3 Product used for unknown indication
126261141 12626114 4 Product used for unknown indication
126261141 12626114 5 Product used for unknown indication
126261141 12626114 6 Product used for unknown indication
126261141 12626114 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126261141 12626114 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126261141 12626114 Brain oedema
126261141 12626114 Bronchial obstruction
126261141 12626114 Cardio-respiratory arrest
126261141 12626114 Coma
126261141 12626114 Hypoxic-ischaemic encephalopathy
126261141 12626114 Intracranial pressure increased
126261141 12626114 Mydriasis
126261141 12626114 Pupils unequal
126261141 12626114 Vomiting

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

no results found

Therapies reported

no results found