Table 3.

Hemoglobin levels and adverse events reported after treatment with anti-D IGIV



Hemoglobin level, g/dL

Adverse events experienced after treatment
Case no.
Before treatment
After treatment
Decrease in hemoglobin level, g/dL
Hemoglobinemia*or hemoglobinuria
Renal insufficiency
Dialysis
PRBCs, U
DIC
Death, d§
1   14.0   4.4   9.6   Yes   —   —   ≥ 5  Yes   —  
2   13.2   10.0   3.2   Yes   Yes   —   —   Yes   3  
3   11.0   8.0   3.0   Yes   Yes   —   —   Yes   4  
4   11.1   3.0   8.1   Yes   —   —   > 2  Yes   10  
5   11.1   6.9   4.2   Yes   Yes   Yes   2   Yes   3  
6
 
13.9
 
7.3
 
6.6
 
Yes
 
Yes
 
Yes
 
2
 
Yes
 
3
 


Hemoglobin level, g/dL

Adverse events experienced after treatment
Case no.
Before treatment
After treatment
Decrease in hemoglobin level, g/dL
Hemoglobinemia*or hemoglobinuria
Renal insufficiency
Dialysis
PRBCs, U
DIC
Death, d§
1   14.0   4.4   9.6   Yes   —   —   ≥ 5  Yes   —  
2   13.2   10.0   3.2   Yes   Yes   —   —   Yes   3  
3   11.0   8.0   3.0   Yes   Yes   —   —   Yes   4  
4   11.1   3.0   8.1   Yes   —   —   > 2  Yes   10  
5   11.1   6.9   4.2   Yes   Yes   Yes   2   Yes   3  
6
 
13.9
 
7.3
 
6.6
 
Yes
 
Yes
 
Yes
 
2
 
Yes
 
3
 

— indicates no information available.

*

Increased serum hemoglobin level or anecdotal report of “visibly red serum” (or similar terms).

Positive urine reagent strip test for blood and urinary sediment with fewer RBCs than would correspond to degree of positivity of reagent strip or anecdotal report of “tea-colored urine” (or similar terms).

Number of units of packed red blood cells transfused.

§

Number of days after treatment that patient died.

Available patient medical records incompletely documented.

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