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
4261678 5660307 I 4261678-9 20010101 20031212 20031229 EXP 2003124516 WWS 52 YR F N 200 LBS 20031224

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
4261678 1004484762 PS ZITHROMAX 1 ORAL 250 MG (DAILY), ORAL U U 50670
4261678 1004502919 C ACETAZOLAMIDE 1 U U
4261678 1004502920 C ANALGESICS 2 U U

Indications of drugs used

Event ID DRUG SEQ INDI PT
4261678 1004484762 SKIN DISORDER
4261678 1004502919 BENIGN INTRACRANIAL HYPERTENSION
4261678 1004502920 HEADACHE

Outcome of event

Event ID OUTC COD
4261678 HO
4261678 OT

Reactions reported

Event ID PT
4261678 BRONCHITIS
4261678 DIARRHOEA
4261678 DISORIENTATION
4261678 DRUG INTERACTION
4261678 FEELING ABNORMAL
4261678 HEADACHE
4261678 HEPATIC FAILURE
4261678 PNEUMONIA
4261678 TREATMENT NONCOMPLIANCE
4261678 VISUAL DISTURBANCE

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

Event ID RPSR COD
4261678 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4261678 1004484762 20011101