Search
Home
About FERRLECIT
Iron Deficiency Anemia
Professional Resource Center
Ferrlecit Support Programs
Dosing Reimbursment
Request a Rep/Order Reprints
Contact Us
Full Prescribing Information
Active Iron Management
The Drive Study
 
Clinical Studies/Reviews
 
The following resources are available:
FERRLECIT PK Study
FERRLECIT Single-Dose Study
FERRLECIT Multiple-Dose Study
Safety of FERRLECIT in Dextran-Sensitive Patients Study

 

Click here to request any of these resources

 

 
+ References:
 
Safety Information
FERRLECIT is contraindicated in non iron-deficient anemias, in patients hypersensitive to FERRLECIT or its inactive components, or with evidence of iron overload • Hypersensitivity reactions have been reported with injectable iron products • Hypotension has been reported with rapid administration of IV iron • In a single-dose, placebo-controlled safety study (n=1097), the most frequent adverse events occurring after FERRLECIT administration were hypotension, nausea, and vomiting and/or diarrhea • In multiple-dose studies (n=126), the most frequent adverse events, whether or not related to FERRLECIT administration, were nausea, vomiting and/or diarrhea, injection site pain, hypotension, cramps, hypertension, dizziness, dyspnea, and chest pain • Please see full prescribing information for Warnings, Precautions, and Adverse Reactions
Watson Pharmaceuticals, Inc.