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Index of reports
> Disability (2)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Venofer (Iron Sucrose) disability. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Venofer side effects in 68 year old female
Reported by a pharmacist from United States on 2012-01-30
Patient: 68 year old female, weighing 78.6 kg (172.9 pounds)
Reactions: Acute Pulmonary Oedema
Adverse event resulted in: hospitalization, disablity
Drug(s) suspected as cause:
Venofer
Possible Venofer side effects in 42 year old female
Reported by a health professional (non-physician/pharmacist) from United States on 2011-11-16
Patient: 42 year old female, weighing 78.0 kg (171.6 pounds)
Reactions: Extravasation, Activities of Daily Living Impaired, Injection Site Haemorrhage, Injection Site Reaction, Infusion Site Pain
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Venofer
Other drugs received by patient: Venofer (Iron Sucrose Injection, Usp) (2340-10) (Iron Sucrose Injectio
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