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
6316542 7086586 I 6316542-8 20090618 20090807 20090820 EXP GB-GENENTECH-288715 GNEFDAAERSPRD 12 M Y 55.1 KG 20090820 OT UNITED KINGDOM

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
6316542 1012078062 PS XOLAIR 1 SUBCUTANEOUS 300 MG, UNK NOT REPORTED
6316542 1012078063 SS XOLAIR 1 UNK NOT REPORTED
6316542 1012078064 C SYMBICORT 1
6316542 1012078065 C UNKNOWN DRUG 2
6316542 1012078066 C PREDNISOLONE 1 5 MG, UNK
6316542 1012078067 C CETIRIZINE HCL 1 10 MG, UNK
6316542 1012078068 C IPRATROPIUM BROMIDE 1
6316542 1012078069 C OMEPRAZOLE 1
6316542 1012078070 C AUGMENTIN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6316542 1012078062 DRUG USE FOR UNKNOWN INDICATION
6316542 1012078064 DRUG USE FOR UNKNOWN INDICATION
6316542 1012078065 DRUG USE FOR UNKNOWN INDICATION
6316542 1012078066 DRUG USE FOR UNKNOWN INDICATION
6316542 1012078067 DRUG USE FOR UNKNOWN INDICATION
6316542 1012078068 DRUG USE FOR UNKNOWN INDICATION
6316542 1012078069 DRUG USE FOR UNKNOWN INDICATION
6316542 1012078070 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
6316542 OT

Reactions reported

Event ID PT
6316542 DIZZINESS
6316542 HYPERHIDROSIS
6316542 HYPOAESTHESIA
6316542 PALLOR
6316542 PARAESTHESIA

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6316542 1012078062 20090618
6316542 1012078063 20090723