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
4784338 5888836 F 4784338-4 20050712 20050801 20050930 EXP PHEH2005US08475 NOVARTIS PHARMACEUTICALS CORP. 52 YR F Y 122 KG 20050929 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
4784338 1006470466 SS SANDOSTATIN LAR 1 UNK, UNK
4784338 1006470467 C ZYRTEC 1 20 MG, UNK
4784338 1006470468 C ACIPHEX 1 40 MG, UNK
4784338 1006470469 C ZOFRAN 1 40 MG, PRN
4784338 1006470470 C TRAMADOL 2 50 MG, PRN
4784338 1006470471 C DARVOCET-N 100 1 1 TAB PRN
4784338 1006470472 C PROCRIT /00909301/ 2 40,000 UNITS
4784338 1006470473 C PROCRIT /00909301/ 2 40,000 UNITS
4784338 1006470474 PS SANDOSTATIN 1 UNK, UNK 019667

Indications of drugs used

Event ID DRUG SEQ INDI PT
4784338 1006470466 PANCREATITIS
4784338 1006470467 HYPERSENSITIVITY
4784338 1006470468 GASTROOESOPHAGEAL REFLUX DISEASE
4784338 1006470469 NAUSEA
4784338 1006470470 PAIN
4784338 1006470471 PAIN
4784338 1006470474 PANCREATITIS

Outcome of event

Event ID OUTC COD
4784338 OT

Reactions reported

Event ID PT
4784338 BIOPSY BREAST
4784338 BIOPSY SKIN
4784338 BREAST FIBROSIS
4784338 BREAST MASS
4784338 BREAST PAIN
4784338 BREAST TENDERNESS

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
4784338 1006470466 20050801
4784338 1006470474 20050628