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BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
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BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 1/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Aldesleukin 22 million IU
(1.3 mg) (Novartis) (F)(PFL)
no preservative1
1.2 mL SWI1,2 direct diluent against side of vial during reconstitution1 do not shake1
18 million IU/mL (1.1 mg/mL)1,2
48 h F1
50 mL D5W1
30 – 70 mcg/mL1
< 30 mcg/mL: dilute in
D5W containing human albumin 0.1%2
48 h F1
- cytotoxic3 - do not use in-line filter1,2 - avoid bacteriostatic water for injection or NS due to increased aggregation1
Alemtuzumab 30 mg/mL
(Genzyme previously Bayer)4 (F)(PFL)
do not shake no preservative5
N/A
filter NOT required5
30 mg/mL5
discard unused
portion5
SC syringe6
discard at the end of
the day F or RT
- cytotoxic7 - do not shake8
100 mL NS or D5W5
8 h F or RT5
**(PFL)8
Alemtuzumab 30 mg/3 mL
(Schering/Ilex) (F)(PFL)
do not shake no preservative9
N/A
use 5 micron filter to withdraw drug from ampoule8
10 mg/mL9
discard unused
portion9
SC syringe6
discard at the end of
the day F or RT8
- cytotoxic7 - do not shake8
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 2/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
100 mL NS or D5W9
8 h F or RT8
**(PFL)8
Amifostine 500 mg
(MedImmune) (RT)
no preservative10
9.7 mL NS only10
50 mg/mL10
24 h F, 5 h RT10
25–50 mL*NS only10
5–40 mg/mL:
24 h F,10 5 h RT
- noncytotoxic10 - discard cloudy solution11
Amsacrine 75 mg/1.5 mL (Erfa Canada)
(RT) no preservative12
glass syringes
preferred during reconstitution;
max. time in plastic syringe12: 15 min
13.5 mL supplied diluent (L-lactic
acid)1
transfer 1.5mL from
ampoule into the diluent vial12
5 mg/mL12
24 h RT12
PFL12
500 mL D5W12
(plastic or glass container)12
7 d F, 48 h RT12,13,14
- cytotoxic15
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 3/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Asparaginase16 (asparaginase E. coli)
10,000 units (Orphan
Pharmaceutical International)
(F) no preservative17
do not shake; roll to
reconstitute18,11 4 mL SWI19
Intradermal test11: Reconstitute with
5 mL SWI to give 2000 units/mL
Transfer 0.1 mL to 10 mL vial (or 12 mL syringe)
Add 9.9 mL SWI roll to dissolve to give 20 units/mL
2 unit test dose = 0.1 mL
(Note: the rest of the reconstituted vial
has a concentration of 2000 units/mL)11
2500 units/mL16
48 h F, RT16
syringe16
14 d F20, 16
- cytotoxic3
50 mL*NS or D5W20,13
14 d F,20,13 2 d RT20,21
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 4/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Erwinia asparaginase (asparaginase Erwinia
chrysanthemi) 10,000 units
(Orphan Pharmaceuticals
International) (F)
no preservative22
do not shake; roll to
reconstitute22
1-2 mL NS22
10000-5000
units/mL
15 min in original container; 8 h in a
glass or polypropylene
syringe22
glass or
polypropylene syringe22
8 h in a glass or polypropylene
syringe22
- cytotoxic3
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 5/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
PEG-asparaginase (pegasparagase)
(pegylated asparaginase E. coli)
750 units/mL (Enzon)
(F) no preservative23
N/A
750 units/mL23
discard unused
portion23
IM: maximum volume
2 mL; if >2 mL use multiple sites23
syringe: 4 h23,24
- cytotoxic3 - discard cloudy solution23 - do not shake23 - do not use if stored out of refrigerator for > 48 h23 - do not use if previously frozen23
IV: 100 mL NS or D5W23
bag: 4 h23,24
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 6/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Azacitidine 100 mg
(Celgene) (RT)
no preservative25
4 mL SWI25 shake vigorously25
25 mg/mL25
8 h F,
45 min RT25
SC syringe25
45 min RT25
prepare immediately before use and use
within 45 min, or discard.
- cytotoxic3 - discard if contains large particles25 - re-suspend syringe contents before injection by vigorously rolling syringe between palms25
BCG 81 mg
(Sanofi Pasteur) (F)(PFL)
preservative26
do not shake; roll to
reconstitute26
3 mL supplied diluent26
record time of reconstitution
10.5 ± 8.7×108
CFU/vial (Connaught
strain)26
2 h F, RT26
50 mL NS26
2 h F or RT after reconstitution26
**(PFL)26
- cytotoxic7
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 7/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
BCG (Tice substrain)
50 mg = 1 to 8 x 108 CFU
(Hospira/Organon) (F)(PFL)
no preservative27
1 mL preservative
free NS for injection27
use reconstitution device provided
allow to stand for a few minutes, then
gently swirl to suspend27
1 to 8×108 CFU/vial27
2 h F (PFL)27
transfer from vial to 60 mL syringe, rinse
vial with another 1 mL NS. Add rinse to
same 60 mL syringe. qs to 50 mL with NS27
2 h F27
- cytotoxic3 - overfill unknown - protect from light27 - do not filter27
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 8/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Bendamustine 25 mg single-use vial 100 mg single-use vial
(Cephalon) (RT)(PFL)
no preservative28
25 mg vial: add 5
mL SWI 100 mg vial: add 20
mL SWI28
Shake well to yield a clear, colourless to a pale yellow solution.
Expected to completely dissolve within 5 minutes28
5 mg/mL28
30 minutes28
500 mL NS28
0.2-0.6 mg/mL28
24 h F, 3 h RT28
- cytotoxic3
Bevacizumab 100 mg/4 mL
400 mg/16 mL (Roche) (F)(PFL)
do not shake no preservative29
N/A
25 mg/mL29
discard unused
portion29
1.4-16.5 mg/mL30
100-250 mL NS
only29,30
48 h F, RT21,29,30
- cytotoxic7 - do not shake29
Bleomycin 15 IU
(NB: dose in units only) (Bristol)
(F) no preservative31
6 mL*NS31
2.5 IU/mL
48 h F31
50 mL*NS31
24 h RT31
- cytotoxic7 - no overfill32
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 9/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Bleomycin 15 IU
(NB: dose in units only) (Hospira) (F)(PFL)
no preservative33
6 mL*NS or SWI33
2.5 IU/mL33
48 h F, 24 h RT33
50 mL *NS, SWI33
24 h RT34
- cytotoxic7 - no overfill35
Bortezomib 3.5 mg
(Ortho Biotech formally Millennium) (RT)(PFL)
no preservative36
3.5 mL NS36
1 mg/mL36
2d RT13,37
syringe36
8 h RT38
- cytotoxic7
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 10/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Busulfan 60 mg/10 mL
(Orphan Medical) (F)
no preservative39
N/A
use 5-micron nylon filter provided with
ampoule to withdraw drug39
6 mg/mL39
discard unused
portion39
NS or D5W (dilute in volume 10 times the busulfan volume to ~
0.5 mg/mL)39
complete
administration within 12 h F: NS39
8 h RT: NS, D5W
- cytotoxic7
Carboplatin 50 mg/5 mL
150 mg/15 mL 450 mg/45 mL
(Hospira) (RT)(PFL)
no preservative40
N/A
10 mg/mL40
discard unused
portion40
0.3-10 mg/mL41
NS, D5W11,40
do NOT use
aluminum-containing needle or syringe41
24 h RT,42 48 h F40
- cytotoxic7 - do NOT use aluminum-containing needle, syringe or tubing41
Carboplatin 50 mg/5 mL
150 mg/15 mL 450 mg/45 mL (Novopharm)
(RT)(PFL) no preservative43
N/A
10 mg/mL43
discard unused
portion RT43
0.5-10 mg/mL44
NS, D5W11,43,45
do NOT use
aluminum-containing needle or syringe43
8 h RT43
- cytotoxic7 - do NOT use aluminum-containing needle, syringe or tubing43
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 11/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Carmustine 100 mg
(Bristol Labs) (F)
no preservative46
3 mL diluent (supplied)46
diluent to reach RT, then dissolve drug with 3 mL diluent; add 27 mL SWI46
record time of reconstitution
3.3 mg/mL in 10%
ethanol46
24 h F, 8 h RT46
glass46 or polyolefin
container11
500 mL NS or D5W46
24 h F: in glass,46 or polyolefin container11
use within 4 h of
reconstitution RT46
- cytotoxic7 - do not use if product has oily droplets46
Cetuximab 100 mg/50 mL 200 mg/100 mL (ImClone/BMS)
(F) do not dilute do not shake
no preservative47
N/A
2 mg/mL47
discard unused
portion after 12 h F, 8 h RT47
syringe47
sterile evacuated container or bag e.g.
polyolefin, polyethylene, ethylene vinyl acetate, DEHP
plasticized PVC, PVC bag, or glass47
12 h F, 8 h RT47
12 h F, 8 h RT47
- cytotoxic3 - administer with a 0.2 or 0.22 micron low protein binding in-line filter47 - normal saline may be used to flush the line47 - solution may contain white particulates which do not affect product quality47
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 12/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Cisplatin 10 mg/10 mL 50 mg/50 mL
100 mg/100mL (Hospira) (RT)(PFL)
no preservative48
N/A
1 mg/mL48
48 h RT49
< 60 mg: 100 mL NS*> 60 mg: 250 mL NS*
500 or 1000 mL *NS, D5-NS, D5-1/2S; D5-NS with mannitol; D5-
1/2S with mannitol48,50; D5W-1/3S with mannitol48
do NOT use
aluminum-containing needle or syringe48
48 h RT49
- cytotoxic7 - do NOT use aluminum-containing needle, syringe or tubing48
Cladribine 10 mg/10 mL
(Janssen-Ortho) (F)(PFL)
no preservative51
N/A
1 mg/mL51
discard unused
portion51
SC syringe52
cassette51
48h F, end of day
RT13,51,53,54
- cytotoxic7 - shake vigorously to dissolve any precipitates from refrigeration11 - bacteriostatic NS contains benzyl alcohol51
500 mL NS only51
Do NOT use D5W51
24 h RT51
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 13/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
qs to 100 mL with bacteriostatic NS
only via SIMS DELTEC INC. MEDICATION
CASSETTES®51; filter drug and diluent
through 0.22u filter as each solution is being
introduced into the medication
at least 7 days51
Clodronate 300 mg/10 mL
(Oryx) (RT)
no preservative55
N/A
30 mg/mL
discard unused
portion55
500 mL NS or D5W55
12 h RT55
- noncytotoxic
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 14/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Cyclophosphamide 200 mg 500 mg
1000 mg 2000 mg (Baxter)
(RT)(PFL) no preservative56
NS56
200 mg: 10 mL 500 mg: 25 mL
1000 mg: 50 mL 2000 mg: 100 mL56
20 mg/mL56
72 h F,56,57 24 h
RT56
< 1 g: 100 mL NS* > 1 g: 250 mL NS* high dose in BMT: may need 500 NS*
NS, D5W, D5NS56
72 h F,56,57 24 h RT56
- cytotoxic7
Cyclosporine 50 mg/1 mL 250 mg/5 mL
(Novartis) (RT)(PFL)
no preservative58
N/A
50 mg/mL58
discard unused
portion58
NS, D5W58
dilute to concentration
between 1:20 and 1:10058
dilute immediately prior
to use58
- cytotoxic3 - polyoxyethylated castor oil/ethanol vehicle58 - do NOT refrigerate or freeze58 - use non-PVC bag and tubing59
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 15/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Cytarabine 100 mg/1 mL
1000 mg/10mL 2000 mg/20mL
(Hospira) (RT)(PFL)
no preservative60
N/A
record time of
puncture
100 mg/mL60
24 h RT60
100 mL*NS, Water for
Injection, D5W, Lactated Ringer’s60
72 h F, 24 h RT from initial vial puncture60
- cytotoxic7 - do not use for IT injection
Cytarabine IT injection60 100 mg/1 mL
1000 mg/10mL 2000 mg/20mL
(Hospira) (RT)(PFL)
no preservative60
N/A
record time of
puncture
100 mg/mL60
24 h RT60
diluents containing
preservatives should NOT be used for
intrathecal administration60
qs to 6 mL with
preservative free NS61
use within 4 h of initial
vial puncture11,13
- cytotoxic7 - auxiliary label62: “IT” - label to include route in full (i.e., INTRATHECAL injection) attached to both syringe and outer ziplock bag62
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 16/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Cytarabine SC injection:
100 mg (Pfizer)
(RT)(PFL) no preservative63
100 mg: 5 mL BWI63
100 mg:
20 mg/mL63
48 h RT63,64
syringe
14 d F, 48 h RT64
- cytotoxic7 - for high dose use, do not use diluent containing benzyl alcohol65 - do not use for IT injection
Dacarbazine 100 mg 200 mg
(Abraxis) (F)(PFL)
no preservative66
100 mg: 9.9 mL
SWI66 200 mg: 19.7 mL
SWI66
10 mg/mL66
72 h F, 8 h RT66
250-500 mL*NS or
D5W
24 h F, 8 h RT66
**(PFL)11,66 see Special
Precautions/Notes Column
- cytotoxic7 - protect container from light during storage and administration67 - overfill unknown
Dacarbazine 200 mg 600 mg
(Hospira) (F)(PFL)
no preservative68
200 mg: 19.7 mL
SWI68 600 mg: 59.1 mL
SWI68
10 mg/mL68
48 h F, 8 h RT68
(PFL)69
0.19–3.0 mg/mL13,68
250-500 mL*NS or
D5W
24 h F68
**(PFL)67
see Special Precautions/Notes
Column
- cytotoxic7 - protect container from light during storage and administration67 - no overfill69,35
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 17/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Dactinomycin 0.5 mg
(Ovation)70 (RT)(PFL)
no preservative71
1.1 mL
SWI(preservative free)71
Do NOT use SWI with preservative
(may form precipitate)71
0.5 mg/mL71
(500 mcg/mL)
24 h F, RT72
syringe71,73
24 h F, RT74
- cytotoxic3 - do not filter71,73 .
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Daunorubicin 20 mg
(Erfa Canada Inc.)75 (RT)(PFL)76
no preservative77
4 mL SWI75
5 mg/mL75,78
48 h F, 24 h RT77
100-250 mL in
isotonic solution e.g., NS75
no data for D5W77
24 h RT, 48 h F75
- cytotoxic3
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 18/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Daunorubicin 20 mg
(Novopharm) (RT)(PFL)
no preservative79
4 mL SWI79
5 mg/mL79
24 h RT, 48 h F79
(PFL)79
100-250 mL NS or D5W11
48 h F, 24 h RT79
**(PFL)79
- cytotoxic7
Dexrazoxane 250 mg 500 mg (Pfizer)
(RT) no preservative80
supplied diluent80:
250 mg: 25 mL 500 mg: 50 mL
10 mg/mL80
6 h F80
empty viaflex bag80
6 h RT81
- cytotoxic82
Docetaxel 20 mg/0.5 mL 80 mg/2 mL
(Sanofi-Aventis) (F, RT) (PFL)
no preservative83
supplied diluent :
- if vials were refrigerated, allow to
warm for 5 min at RT. Withdraw entire
contents of the diluent and inject the
entire contents of the syringe into the
corresponding concentrate vial. Mix
by repeated inversions for 45 sec
DO NOT SHAKE Let sit for 5 minutes83,84
10 mg/mL83
48 h F, RT13,85
0.3–0.74 mg/mL
(e.g., 250 mL NS or
D5W)83
complete
administration within 4 h F,83 48 h RT86,87
- cytotoxic7 - non-PVC bag and tubing only83
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 19/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Doxorubicin
10 mg 50 mg 150 mg
(Hospira) (RT)(PFL)
no preservative88
NS, SWI, D5W88
(NS reconstitution takes longer) 10 mg: 5 mL 50 mg: 25 mL 150 mg: 75 mL
2 mg/mL88
48 h F, 24 h
RT13,88
syringe88
48 h F, 24 h RT13,89
- cytotoxic7
0.2–2 mg/mL90
100 mL*NS88
48 h F, 24 h RT13,90
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 20/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Doxorubicin 10 mg/5 mL 20 mg/10 mL 50 mg/25 mL
200 mg/100 mL (Novopharm)
(F)(PFL) no preservative91
N/A
record time of
puncture
2 mg/mL
8 h91
syringe91
48 h F, 24 h RT91
from initial vial puncture
- cytotoxic7
Doxorubicin 10 mg/5 mL 50 mg/25 mL
200 mg/100 mL (Pfizer)
(F) no preservative92
N/A
2 mg/mL92
discard unused
portion92,74
syringe92
48 h F, 24 h RT92
- cytotoxic3
Doxorubicin Pegylated Liposomal
20 mg/10 mL 50 mg/25 mL
(Schering) (F)
no preservative93
N/A
2 mg/mL93
discard unused
portion93
< 90 mg: 250 mL
D5W only93
≥ 90 mg: 500mL D5W only
24 h F93
- cytotoxic7 - do not filter93
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 21/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Epirubicin 10 mg/5 mL 50 mg/25 mL
200 mg/100 mL (Pfizer) (F)(PFL)
no preservative94
N/A
record time of
puncture
2 mg/mL94
8 h94
syringe94
48 h F, 24 h RT from initial vial puncture94
- cytotoxic7
100 mL*NS or D5W11
2 d F, RT: NS or
D5W49
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 22/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Etoposide 100 mg/5 mL
500 mg/25 mL 1000 mg/50 mL
(BMS) (RT)
preservative95
N/A
20 mg/mL95
14 d RT11,13,96,97,98
0.2– 0.4 mg/mL95
500 mL*NS or D5W95
0.2 mg/mL: 48 h RT13,95 0.4 mg/mL: 24 h RT95
- cytotoxic7 - use non-PVC bag and tubing only
Etoposide 100 mg/5 mL
200 mg/10 mL 500 mg/25 mL 1000 mg/50 mL
(Novopharm) (RT)(PFL)
no preservative99
N/A
20 mg/mL99
discard unused
portion99
NS
Stabilty is
concentration dependent
0.2-0.3 mg/mL: 7 d F,100 2 d RT87,100 0.4-0.5 mg/mL: 1 d F,100 1 d RT100 0.6-9.0mg/mL: generally unstable100 9.5 mg/mL: 2 d F,100 1d RT100 10-12 mg/mL: 7 d F,100 2 d RT87,100
- cytotoxic7 - use non-PVC bag and tubing only
D5W99
4 h RT99,101
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 23/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Fludarabine 50 mg
(Berlex) (F)
no preservative102
2 mL SWI102
25 mg/mL102
48 h F or RT13,49
dilute to maximum of
1 mg/mL102,103
100 mL*NS or D5W102
48 h F, RT13,49
- cytotoxic7
Fludarabine 50 mg
(Novopharm) (F)
no preservative104
N/A
25 mg/mL104
discard unused
portion104
dilute to maximum of
1 mg/mL104
100 mL*NS or D5W
48 h F, 24 h RT104
- cytotoxic7
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 24/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Fluorouracil 5000 mg/100 mL
(Hospira) (RT)(PFL)
no preservative105
N/A
50 mg/mL105
8 h RT105,106
syringe13
48 h RT13,21,106
- cytotoxic7
2-10 mg/mL in
D5W105,106
50-1000 mL*D5W
24 h RT105,106
CIVI: ambulatory
pump106
complete within
8 d11,13,107
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 25/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Gemcitabine 200 mg
1000 m g (Eli-Lilly)
(RT) no preservative108
200 mg: 5 mL NS 1000 mg: 25 mL
NS108
38 mg/mL108
48 h RT108,109
syringe108
48 h RT,13,108,109
- cytotoxic7
0.1–10 mg/mL
NS108,109
48 h F, RT13,108,109
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 26/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Gemcitabine 200 mg
1000 mg 2000 mg (Hospira)
RT110 no preservative111
200 mg vial: 5 mL
NS 1000 mg vial: 25 mL
NS 2000 mg vial: 50 mL
NS110
38 mg/mL110
48 RT110,112,74
syringe110
24 h RT110,112
- cytotoxic7
26 mg/mL-0.1 mg/mL
NS110,112
48 h RT112,74
Gemcitabine 200 mg
1000 mg (Novopharm)
RT no preservative113
200 mg vial: 5mL
NS 1000 mg vial: 25 mL
NS114
38 mg/mL114
24 h RT114
38 mg/mL – 0.1
mg/mL NS114
24 RT114
- cytotoxic7
Gemcitabine 200 mg
1000 mg (Sandoz Standard)
RT no preservative115
200 mg vial: 5 mL
NS 1000 mg vial: 25 mL
NS115
38 mg/mL115
48 h RT115,116
syringe115
48 h RT115,117,116
- cytotoxic7
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 27/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
38 mg/mL-0.1 mg/mL
NS or D5W115,118
48 h RT13,119
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 28/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Idarubicin 5 mg
10 mg (Pfizer)
(RT)(PFL) no preservative120
vial under negative
pressure120
5 mg: 5 mL SWI 10 mg: 10 mL
SWI120
1 mg/mL120
48 h F,120 24 h RT
(PFL)120
syringe
48 h F,13, 120 24 h RT13
(PFL)120
- cytotoxic7
Idarubicin 5 mg/5 mL
10 mg/10 mL 20 mg/20 mL
(Pfizer) (F)(PFL)
no preservative120
N/A
1 mg/mL120
same as
reconstituted solution121
syringe
Discard 48 h F,13,120 24 h RT13
(PFL)120
- cytotoxic7
Ifosfamide 1000 m g 3000 mg (Baxter) (RT) 11
no preservative122
1000 mg: 20 mL
SWI122 3000 mg: 60 mL
SWI
shake well
50 mg/mL122
48 h F13,122
0.6–20 mg/mL122
500–1000 mL*NS,
D5W, D5-NS, D5-1/2NS, Lactated
Ringer’s11,122
72 h F122
24 h F, RT when mixed with mesna11
D5W or Lactated
Ringer’s when mixed
- cytotoxic7
Interferon Alfa -2b 18 million IU/3 mL
(Schering) (F)(or up to 7 days at
RT before use) no preservative123
N/A
6 million IU/mL123
48 h F13,123
syringe123
2 d F13,124
- cytotoxic7
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 29/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
≥ 0.3 million IU/mL123
50 mL NS123
24 h F, RT124
Interferon Alfa -2b 25 million IU/2.5 mL
(Schering) (F)(or up to 7 days at
RT before use) no preservative123
N/A
10 million IU/mL123
48 h F13,123
syringe123
2 d F13,124
- cytotoxic7
≥ 0.3 million IU/mL123
50 mL NS123
24 h F, RT124
Interferon Alfa -2b 10 million IU (Schering)
(F) no preservative123
1 mL supplied
diluent (SWI) 123
do not shake; roll to reconstitute123
10 million IU/mL123
24 h F123
syringe123
24 h F, RT124
- cytotoxic7
> 0.1 million IU/mL124
100 mL NS125
48 h RT11,13
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 30/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
1 mL BWI123
do not shake; roll to
reconstitute123
48 h F, RT13,123
syringe125
14 d F, 48 h RT13,125
100 mL NS125
48 h RT11,13
Interferon Alfa -2b 18 million IU (Schering)
(F) no preservative123
1 mL supplied
diluent123
do not shake; roll to reconstitute123
18 million IU/mL123
24 h F123
syringe123
24 h F, RT124
- cytotoxic7
> 0.1 million IU/mL126
100 mL NS125
48 h RT11,13
1 mL BWI123
do not shake; roll to
reconstitute123
48 h F, RT13
syringe123
14 d F13,125
100 mL NS125
48 h RT11,13
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 31/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Irinotecan 40 mg/2 mL 100 mg/5 mL
500 mg/25 mL (Hospira) (RT)(PFL)
no preservative127
N/A
20 mg/mL127
2 days RT13,128,129
0.12– 2.8 mg/mL127
500 mL11 D5W
(preferred), NS127
24 h RT: D5W, NS127
48 h F: D5W
(PFL)127
- cytotoxic7 - do NOT refrigerate if in NS130
Irinotecan 40 mg/2 mL 100 mg/5 mL
(Pfizer) (RT)(PFL)
no preservative130
N/A
20 mg/mL130
discard unused
portion130
0.12– 2.8 mg/mL130
500 mL11 D5W
(preferred), NS130
24 h RT: D5W, NS130
48 h F: D5W
(PFL)130
- cytotoxic7 - do NOT refrigerate if in NS130
Irinotecan 40 mg/2 mL 100 mg/5 mL
(Sandoz) (RT)(PFL)
no preservative131
N/A
20 mg/mL131
discard unused
portion131,74
0.12-2.8 mg/mL131
D5W (recommended)
NS131
24 h RT: D5W NS131
48 h F: D5W131
(PFL)131
- cytotoxic3
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 32/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Ixabepilone 15 mg
(contains 16 mg) 45 mg
(contains 47 mg) (BMS)
(F)(PFL) no preservative132
8 mL supplied
diluent
23.5 mL supplied diluent
2 mg/mL
2 mg/mL
1 h RT132
0.2 – 0.6 mg/mL in Lactated Ringer’s Injection USP (use non-PVC infusion
container)132
6 h RT132
- cytotoxic3 - use 0.2-1.2 micron in-line filter132 - use non-PVC (i.e., DEHP-free) administration set132
Leucovorin 50 mg/5 mL
500 mg/50 mL (Hospira) (F)(PFL)
no preservative133
N/A
10 mg/mL133
5 mL vial: discard unused portion133
50 mL vial: 8 h
syringe134
7 d F134
48 h RT87,134
- noncytotoxic
0.05-10 mg/mL133
24 h RT133: NS, D5W,
Lactated Ringer’s, Ringer’s
50-250 mL* NS, D5W, Lactated
Ringer’s, Ringer’s, D10W, D5-NS
8 h RT133: D10W, D5-
NS
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 33/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Leucovorin 50 mg/5 mL
500 mg/50 mL (Novopharm) (F)(PFL)135
N/A135
10 mg/mL135
5 mL vial: discard unused portion135
50 mL vial:
discard unused portion135
syringe
8 h135,13
- noncytotoxic
0.060-1.0 mg/mL135
24 h RT NS, Lactated Ringer’s, Ringer’s135
50-250 mL* NS, D5W, Lactated
Ringer’s, Ringer’s, D10W, D10NS135
12 h RT D5W,
D10W135
6 h RT D5NS135
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 34/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Mechlorethamine 10 mg
(Ovation Pharmaceuticals/Merck)
no preservative136
do NOT use if
discoloured or water droplets form in vial
before reconstitution136
10 mL SWI or NS136
record time of reconstitution
1 mg/mL136
use within 4 h of
reconstitution RT11,13
syringe136
complete
administration 4 h of reconstitution
RT11,13,136
- cytotoxic7
100 mL NS49,136
complete
administration within 4 h of reconstitution
RT13,49,136
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 35/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Medroxyprogesterone 250 mg/5 mL
(Pfizer) (RT)
preservative18
N/A
record time of
puncture
50 mg/mL18
use within 4 h of
initial puncture11,137
syringe: IM only18
use within 4 h of initial
vial puncture11,137
- cytotoxic7 - auxiliary label: shake before use18
Medroxyprogesterone Depo
150 mg/1mL (Pfizer)
(RT) preservative18
N/A
record time of
puncture
150 mg/mL18
use within 4 h of
initial puncture11,137
syringe: IM only18
use within 4 h of initial
puncture11,137
- cytotoxic7 - auxiliary label: shake before use18
Melphalan 50 mg (GSK)
(RT)(PFL) no preservative138
10mL supplied
diluent138
immediately after adding diluent,
shake vigorously138
record time of reconstitution
5 mg/mL138
2 h RT138
do NOT
refrigerate
0.1– 0.45 mg/mL in
NS only138
(e.g., > 45 mg and < 110 mg in 250 mL
NS)*
complete
administration within 60 min from time of
initial reconstitution at RT11
- cytotoxic7
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 36/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
Mesna 1000 mg/10mL
(PPC) (RT)
preservative139
N/A
100 mg/mL139
14 d F, RT13,139
> 1mg/mL139
NS or D5W
48 h F, 24 h RT139
- noncytotoxic
Methotrexate 50 mg/2mL
500 mg/20mL 1 g/40mL 5 g/200mL (Hospira) (RT)(PFL)
no preservative140
N/A
25 mg/mL140
50mg: discard
unused portion140
500mg, 1 g, 5 g: 8 h F, RT140
syringe
2 d F, RT11,141,142
- cytotoxic7 - for high-dose regimens (e.g., 1-8 g/m2 as a single dose)143 use preservative-free methotrexate11 - do not use for IT injection
0.4–2 mg/mL140
100 mL* NS, D5W
high dose (e.g., 1-8
g/m2 as a single dose)143,144-146: 500–
1000 mL*
24 h RT140
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 37/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
Methotrexate IT Injection140:
Only preservative free methotrexate may be administered by the intrathecal route140
50 mg/2mL147 (Hospira) (RT)(PFL)
no preservative140
N/A
25 mg/mL140
discard unused
portion140
qs to 6 mL with
preservative free NS61
use within 4 h of initial
puncture11,13
- cytotoxic7 - auxiliary label62: “IT” - label to include route in full (i.e., INTRATHECAL injection) attached to both syringe and outer ziplock bag62
Methotrexate 50 mg/2mL
500 mg/20mL (Hospira) (RT)(PFL)
preservative140
N/A
25 mg/mL140
24 h F141
syringe
14 d F87,141
- cytotoxic7 - high-dose regimen(e.g., 1-8 g/m2 as a single dose)144-146: use preservative-free methotrexate11 - do not use for IT injection
0.4–2 mg/mL140
e.g., 100 mL*NS,
D5W140
4 h RT140
Mitomycin 5 mg
20 mg (Novopharm)
(RT)(PFL) no preservative148
SWI
5 mg: 10 mL 20 mg: 40 mL
shake well148
0.5 mg/mL148
48 h F, RT13,148
(PFL)148
syringe13
14 d F, 48 h RT13,148
- cytotoxic7
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 38/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
0.02-0.04 mg/mL148
NS, D5W, sodium
lactate148
3 h RT: D5W 12 h RT: NS
24 h RT: sodium lactate148
Mitomycin 5 mg
20 mg (BMS)
(RT)(PFL) no preservative149
SWI
5 mg: 10 mL 20 mg: 40 mL
shake well149
0.5 mg/mL149
48 h F, RT13,149
(PFL)149
syringe11
14 d F, 48 h RT11,21
- cytotoxic7
0.02–0.04 mg/mL
NS, D5W, sodium
lactate149
12 h RT: NS
3h: D5W 24 h: sodium lactate149
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 39/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Mitoxantrone 20 mg/10 mL
25 mg/12.5 mL (Hospira) (RT)(PFL)
no preservative150
N/A
2 mg/mL150
discard unused
portion150
0.2-0.6 mg/mL150
NS, D5W150
> 50 mL*150
NS: 24 h F, RT150
**(PFL)150
- cytotoxic7
Mitoxantrone 20 mg/10 mL (Novopharm)
(RT)(PFL) no preservative151
N/A
2 mg/mL151
discard unused
portion151
NS, D5W151
> 50 mL*151
24 h RT151
**(PFL)152
- cytotoxic7
Mitoxantrone 20 mg/10 mL
(Pharmaceutical Partners of Canada)
(RT) no preservative153
N/A
2 mg/mL153
discard unused
portion153
NS, D5W2
> 50 mL*153
24 h RT153
- cytotoxic7
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 40/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
Octreotide 50 mcg/mL; 100
mcg/mL; 500 mcg/mL (Novopharm)
(F)(PFL) no preservative
multidose vials (5mL): 200 µg/mL (F)(PFL)
preservative154
N/A
50 mcg/mL
100 mcg/mL 500 mcg/mL154
discard unused
portion154
sc syringe154
single use vials: use
within 4 h multidose vials: use within 14 d F74,154
- noncytotoxic
200 mcg/mL154
14 d F74,154
infusion: NS154
single use vials or
multidose vials: 24 h RT154
Octreotide (Sandostatin)
1000 mcg/5 mL (Novartis) (F)(PFL)
preservative18
N/A
200 mcg/mL18
discard unused
portion155
50–200 mL NS18,11,156
SC infusion: adjust volume to ensure infusion rate of 25
mcg/h18
24 h RT18
- noncytotoxic10
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 41/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Octreotide (Sandostatin) 50 mcg/1 mL
100 mcg/1 mL 500 mcg/1 mL
(Novartis) (F)(PFL)
no preservative18
N/A
50 mcg/mL
100 mcg/mL 500 mcg/mL18
discard unused
portion18
50-100 mL11,156
NS18
SC infusion: adjust volume to ensure infusion rate of 25
mcg/h18
24 h RT18
- noncytotoxic10
Octreotide (Sandostatin LAR)
10 mg 20 mg 30 mg
(Novartis) (F)(PFL)
preservative155
2 mL supplied
diluent
gently run 2 mL down sides of the
vial; do NOT disturb for 2–5 min, then swirl moderately18
record time of reconstitution
10 mg: 5 mg/mL 20 mg: 10 mg/mL
30 mg: 15 mg/mL18
discard unused
portion18
deep intragluteal
administration only18
use within 4 h of initial
reconstitution18,13
- noncytotoxic10 - do NOT shake
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 42/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Oxaliplatin 50 mg/10 mL
100 mg/20 mL 200 mg/40 mL
(Sanofi-Aventis) (RT)(PFL)
no preservative157
N/A
5 mg/mL157
discard unused
portion157
0.2-1.3 mg/mL158
1.3–2 mg/mL157,158
250–500 mL D5W157
do NOT use NS or
other chloride-containing solution157
do NOT use
aluminum-containing needle and syringe157
0.2-1.3 mg/mL:
14 d F, 48 h RT159,87,158
1.3-2 mg/mL: 48 h F, 24 h RT157
- cytotoxic7 - do NOT use aluminum-containing needle, syringe or tubing157
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 43/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Oxaliplatin 50 mg 100 mg
(Sigmacon) (RT)
no preservative160
SWI, D5W:
50 mg: 10 mL 100 mg: 20 mL
do NOT use NS or
other chloride-containing solution160
do NOT use aluminum-
containing needle and syringe160
5 mg/mL160
24 h F160
500 mL D5W
do NOT use NS or
other chloride-containing solutions
(degrades)160
do NOT use aluminum-containing needle and syringe160
24 h F, 6 h RT160
- cytotoxic7 - do NOT use aluminum-containing needle, syringe or tubing160
Paclitaxel 30 mg/5 mL
100 mg/16.7 mL 300 mg/50 mL
(Biolyse) (RT)161
no preservative
N/A
6 mg/mL162
8 h RT162
- cytotoxic7 - use non-PVC bag and tubing with in-line filter162
0.3–1.2 mg/mL in NS, D5W162 (e.g., 100–1000 mL)*
0.1 mg/mL in NS163 0.012-0.1 mg/mL164
0.3-1.2 mg/mL: 24 h RT162 0.1 mg/mL: 44 h F, RT163 0.012-0.09 mg/mL: 16 h RT164
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 44/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
Paclitaxel 30 mg/5 mL
100 mg/16.7 mL 300 mg/50 mL
(BMS) (RT)(PFL)
no preservative165
N/A
6 mg/mL165
30 mg: 48 h
RT13,165 100 mg: 48 h
RT13,165 300 mg: 24 h
RT165
0.3–1.2 mg/mL in NS, D5W, D5-NS, D5 in
Ringer’s165
(e.g.,100–1000 mL)*
24 h RT165
- cytotoxic7 - use non-PVC and tubing with in-line filter165
0.1–1 mg/mL in NS,
D5W166
Devices with spikes e.g., chemo
dispensing pins, should not be used
with paclitaxel vials165
48 h F, RT166
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 45/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Paclitaxel, nab 100 mg paclitaxel and approximately 900 mg
human albumin (Abraxis Oncology)
(RT)(PFL) no preservative167
inject 20 mL NS over > 1 min (a
chemo pin may be used)168
- direct flow to INSIDE vial wall
- stand solution for > 5 min
- gently swirl and/or invert vial
slowly for > 2 min167
5 mg/mL167
8 h F, PFL167
in empty
sterile PVC or non-PVC infusion
bag167,168
8 h RT167
- cytotoxic167 - do NOT filter167 - non-PVC tubing is NOT needed - the use of an in-line filter is not recommended168
Pamidronate 30 mg/10 mL 60 mg/10 mL 90 mg/10 mL
(Hospira) (RT)
no preservative169
N/A
3 mg/mL 6 mg/mL
9 mg/mL169
discard unused
portion169
0.06–0.36 mg/mL NS,
D5W169
do NOT mix with calcium containing
solution (e.g., Ringer’s)169
e.g., 250 mL NS170
24 h F followed by 24 h
RT (total 48 h)169
**(PFL)169
- noncytotoxic171
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 46/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
Pamidronate 30 mg/10 mL 60mg/10 mL 90 mg/10 mL
(Sandoz Canada) RT
no preservative172
N/A172
3 mg/mL 6 mg/mL
9 mg/mL172
discard unused
portion172,74
NS or D5W172
do NOT mix with
calcium containing solution (e.g., Ringer’s)172
24 h RT172
- noncytotoxic171
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 47/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Panitumumab 100 mg/5 mL
200 mg/10 mL 400 mg/20 mL
(Amgen) (F)(PFL)
do not shake no preservative173
N/A
20 mg/mL173
discard unused
portion173
≤1000 mg: 100 mL
NS173
>1000mg: 150 mL NS173
1-10mg/mL173,174
24 h F, 6 h RT173,174
- cytotoxic3 - administer with 0.2 or 0.22 micron low protein binding in-line filter173 - solution may contain particulates which do not affect product quality173 - do not administer if discoloured173
Pemetrexed 100 mg 500 mg (Eli Lilly)
(RT) no preservative175
100 mg: 4.2 mL
preservative-free NS
500 mg: 20 mL preservative-free
NS175
25 mg/mL175
24 h F, RT175
100 mL
preservative-free NS175
do NOT mix with calcium containing
solution (e.g., Ringer’s)176
24 h F, RT175
- cytotoxic7
Porfimer 15 mg 75 mg
(Axcan) (RT)(PFL)
no preservative177
6.6 mL D5W
31.8 mL D5W177
record time of reconstitution
2.5 mg/mL177
24 h F
(PFL)177
syringe177
use within 4 h of initial
reconstitution13,178
**(PFL)177
- noncytotoxic7 - avoid contact with skin and eyes; protect exposed area from light177
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 48/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
Raltitrexed 2 mg
(AstraZeneca) (F, RT)(PFL)
no preservative179
4 mL SWI179
0.5 mg/mL179
24 h F, RT179
50–250 mL NS,
D5W179
24 h F, RT179
- cytotoxic7
Raltitrexed 2 mg
(Hospira) (F, RT)(PFL)
no preservative180
4 mL SWI180
0.5 mg/mL180
24 h F, RT180
50–250 mL NS,
D5W180
24 h F, RT180
- cytotoxic3
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 49/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Rituximab 100 mg/10 mL 500 mg/50 mL
(Roche) (F)(PFL)
no preservative181
N/A
10 mg/mL181
discard unused
portion181
1–4 mg/mL in NS,
D5W) 181
(e.g., 500 mg/250 mL, 1000 mg/500 mL)*
24 h F + additional 12
h RT181
- noncytotoxic3
syringe182
48 h F, 24 h RT182
Streptozocin 1g
(Pfizer) (F)(PFL)
no preservative182
9.5mL NS, SWI,
D5W182
100 mg/mL182
48 h F,182 24 h RT
50-500 mL*NS, D5W,
SWI182
48 h F, 24 h RT182
- cytotoxic7
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 50/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Temozolomide 100 mg
(Schering) (F)
do not dilute183 do not shake183
no preservative183
41 mL SWI183
2.5 mg/mL183
14 h F, RT183
empty 250 mL PVC
bag183
14 h RT183
- cytotoxic{3
Temsirolimus 30 mg/1.2 mL
(Wyeth) (F)(PFL)184,185
no preservative186
1.8 mL supplied
diluent184,185
10 mg/mL184,185
24 h RT184,185
(PFL)184
250 mL NS184,185
Complete
administration within 6 h184,185
- cytotoxic3 - use non-PVC bag and non-PVC tubing with in-line filter184,185
Teniposide 15 mg/1.5 mL
(Bristol) (RT)
preservative18
N/A
10 mg/mL18
discard unused
portion18
0.1, 0.2, 0.4, or 1 mg/mL in NS or
D5W18
0.1, 0.2, 0.4mg/mL: 24
h RT18
1 mg/mL: complete administration within 4h of preparation18
- cytotoxic7 - do NOT refrigerate18 - use non-PVC bag and tubing18
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 51/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Thiotepa 15 mg
(Bedford) (F)(PFL)
no preservative187
1.5 mL SWI187
filter through 0.22
micron filter187 record time of reconstitution
10 mg/mL187
8 h F187
50 mL* NS187
use within 4 h of initial
reconstitution188,187 **(PFL)187,189
- cytotoxic7 - do not use if precipitates or remains opaque187 - do not use for IT injection
syringe: reconstituted solution is hypotonic and must be further diluted with NS prior
to use187 (final concentration of 0.5-1
mg/ml is nearly isotonic)190
use within 4 h of initial reconstitution188,187 **(PFL)187,189
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 52/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Thiotepa IT injection:
15 mg (Bedford) (F)(PFL)
no preservative187
diluents containing
preservatives should NOT be used for
intrathecal administration
1.5 mL SWI187
filter through 0.22
micron filter187 record time of reconstitution
10 mg/mL187
8 h F187
qs to 6 mL with
preservative free NS191
use within 4 h of initial
reconstitution188,187 **(PFL)187,189
- auxiliary label61 “IT” - label to include route in full (i.e., INTRATHECAL injection) attached to both syringe and outer ziplock bag61 - cytotoxic7 - do not use if precipitates or remains opaque187
Thyrotropin alfa 1.1 mg
(Genzyme) (F)(PFL)
no preservative192
1.2 mL SWI192
swirl contents192; do
not shake
0.9 mg/mL192
24 h F192
syringe192
24 h F192
- noncytotoxic
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 53/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Tocilizumab 80 mg/4 mL
200mg/10 mL 400 mg/20 mL (Genentech)
(F)(PFL) no preservative193
N/A
20 mg/mL193
6 h193, 21
100 mL NS
dilute to 100 mL final volume by withdrawing volume of NS from 100 mL bag equal to volume of drug required for dose prior to adding drug193
24h F193; 6 h RT194
- cytotoxic3 - to prevent foaming: slowly add drug to infusion bag and gently invert bag to mix193
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 54/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Topotecan 4 mg
(GSK) (RT)(PFL)
no preservative195,196
4 mL SWI195
1 mg/mL195
24 h F, RT195
0.01–0.5 mg/mL197
50 mL NS, D5W195
24 h F, RT195
- cytotoxic7
Topotecan 4 mg
(GSK) (RT)(PFL) single use
no preservative198
4 mL SWI198
1 mg/mL198
24 h F, RT198
0.020 – 0.5 mg/mL198
24 h F, RT198
cytotoxic3
Trastuzumab 440 mg (Roche)
(F) preservative199
20 mL supplied BWI
swirl vial gently; allow to stand
undisturbed for 5 min199
21 mg/mL199
14 d F13,199
250mL NS199
do NOT use dextrose containing solutions199
24 h F, RT199
- noncytotoxic3 - do NOT shake199
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 55/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Treosulfan 1 g 5 g
(medac) (RT)
no preservative200
pre-heat SWI to 30°C (not higher) shake vial carefully before adding the warmed SWI 1 g vial: 20 mL SWI, while slightly shaking vial and syringe; continue shaking the reconstituted solution for another 2 min{{10494}} 5 g vial: 100 mL SWI, while slightly shaking vial and syringe; continue shaking the reconstituted solution for another 2 min200
50 mg/mL200
48 h RT13,200
undiluted201
dilute with NS or D5W in empty infusion bag for final concentration
= 20 mg/mL200
48 h RT13,200
- cytotoxic3 - compatible with polytetrafluoroethylene filters200 - may require vigorous shaking to reconstitute200
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 56/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Vinblastine 10 mg/10 mL
(Hospira) (F)(PFL)
no preservative154
N/A
1 mg/mL154
discard unused
portion154
syringe11,154
4 h F, RT202,203
- cytotoxic7 - label with: WARNING: FOR INTRAVENOUS USE ONLY – FATAL IF GIVEN BY OTHER ROUTES204,205
100–250 mL NS, D5W206
24 h F, RT202,203
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 57/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Vincristine 2 mg/2 mL 5 mg/5 mL (Hospira) (F)(PFL)
no preservative207
N/A
1 mg/mL207
8 h F, RT207
50 mL*NS, D5W207
24 h F, 6 h RT,207
**(PFL)207
- cytotoxic7 - label with: WARNING: FOR INTRAVENOUS USE ONLY – FATAL IF GIVEN BY OTHER ROUTES204,205
Vincristine 1 mg/1 mL 2 mg/2 mL 5 mg/5 mL
(Novopharm) (F)(PFL)
preservative208
N/A
1 mg/mL208
14 d F, RT208
50 mL*NS, D5W208
72 h F, 24 h RT65
**(PFL)208
- cytotoxic7 - label with: WARNING: FOR INTRAVENOUS USE ONLY – FATAL IF GIVEN BY OTHER ROUTES204,205
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 58/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
Vinorelbine 10 mg/1 mL 50 mg/5 mL
(GSK) (F)(PFL)
no preservative209
N/A
10 mg/mL209
discard unused
portion209
syringe: 1.5 – 3.0 mg/mL in NS or
D5W209
24 h F, RT209
- cytotoxic7 - label with: WARNING: FOR INTRAVENOUS USE ONLY – FATAL IF GIVEN BY OTHER ROUTES204,205
0.5 – 2.0 mg/mL209
50 mL*NS, D5W, ½NS, D5½NS,
Ringer’s, Ringer’s Lactate209
24 h F, RT209
Vinorelbine 10 mg/1 mL 50 mg/5 mL
(Hospira) (F)(PFL)
no preservative210
N/A
10 mg/mL210
discard unused
portion210
syringe: 1.5 – 3.0 mg/mL in NS or
D5W210
24 h F, RT210
- cytotoxic7 - label with: WARNING: FOR INTRAVENOUS USE ONLY – FATAL IF GIVEN BY OTHER ROUTES204,205
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 59/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
DRUG & STRENGTH (Storage Prior to Use,
Manufacturer, Preservative Status)
Reconstitute With:
To Give: Vial Stability
Product Product Stability Special Precautions/Notes
0.5 – 2.0 mg/mL210
50 mL* NS, D5W,
½NS, D5½NS, Ringer’s, Ringer’s
Lactate210
24 h F, RT210
Vinorelbine 10 mg/1 mL 50 mg/5mL
(Pierre Fabre Pharma Canada) (F)(PFL)
no preservative211
N/A211
10 mg/mL211
discard unused
portion211
syringe: 1.5-3.0
mg/mL in D5W or NS211
24 h F, RT211
- cytotoxic3 - label with: WARNING: FOR INTRAVENOUS USE ONLY – FATAL IF GIVEN BY OTHER ROUTES204,205
0.5-2.0 mg/mL211
NS, D5W, ½NS,
D5½NS, Ringer’s, Ringer’s Lactate211
24 h F, RT211
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 60/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 61/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
* Suggested volume based on usual dose range and any concentration range of stability data ** Protect from light means minimizing exposure to direct sunlight over a storage period. More specific information on protection from light (eg, protecting container and tubing during administration) will be indicated in the Under the Special Precautions/Notes column. Centres are not to change the content locally but should forward suggestions to the Cancer Drug Manual staff. Explanatory Notes Stability data assume products prepared using standard aseptic technique in biological safety cabinet at low risk for contamination according to the classification outlined in USP 797.21,212 Vial stability: Stability of solution after first puncture or reconstituted solution Storage temperature: If information states same stability with refrigerator and room temperature storage, then bold refrigerated as preferred (ie, to minimize growth of micro-organisms). Cytotoxic: hazardous (see Policy II-20 for more details). Discard unused portion: Unused portion from single use vials should be discarded at the end of the day. State “overfill known” if the manufacturer states overfill within acceptable limits is present. PFL = protect from light RT = room temperature F = refrigerated SWI = sterile water for injection NS = normal saline D5W = dextrose 5% BWI = bacteriostatic water for injection
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 62/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
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BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 63/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
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BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 64/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
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36. Millenium Pharmaceuticals Inc. Velcade product monograph. Cambridge, Massachusetts; May 2003.
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BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 65/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
40. Mayne Pharma (Canada) Inc. Carboplatin Package Insert. Montreal, QC; Undated.
41. Nancy Grioriadis. Personal communication. Regulatory Affairs Associate, Mayne Pharma (Canada) Inc. 2 October 2006.
42. Nancy Griogoriadis. Personal communication. Regulatory Affairs Associate, Mayne Pharma (Canada) Inc. 2 October 2006.
43. Novopharm Limited. Carboplatin Package Insert. Toronto, Canada; Undated.
44. Manjinder S Kang. Personal communication. Regulatory Affairs Drug Information Pharmacist, Novopharm Canada. 14 March 2005.
45. Repchinsky C. Paraplatin-AQ, Compendium of Pharmaceuticals and Specialties. 12th ed. Ottawa, Ontario: Canadian Pharmacists Association; 2004.
46. Bristol Laboratories of Canada. BiCNU Package Insert. Montreal, Canada; 2002.
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51. Janssen-Ortho Inc. LEUSTATIN® Product Monograph. Toronto, Ontario; 31 July 2006.
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 66/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
53. Myrna O'Brodovich. Personal communication. Senior Medical Information Associate Ortho Biotech; 2 April 2008.
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55. Oryx Pharmaceuticals Inc. Clasteon Product Monograph. Mississauga, Ontario; 25 November 2004.
56. Baxter Corporation. Procytox Package Insert. Toronto, Ontario; 2004.
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60. Mayne Pharma (Canada) Inc. Cytarabine Injection Product Monograph. Montreal, Quebec; 25 July 2003.
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63. Pfizer Canada Inc. CYTOSAR® Sterile Powder Product Monograph. Kirkland, Quebec; 17 March 2004.
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BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 67/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
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BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 68/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
79. Novopharm Limited. Daunorubicin Package Insert. Toronto, Canada; Undated.
80. Pharmacia & Upjohn Inc. Zinecard Package Insert. Mississauga, Ontario; 2004.
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90. John Korontzis. Personal communication. Regulatory Affairs Associate, Doxorubicin, Mayne Pharma Canada; February 2005.
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92. Pfizer Canada Inc. Adriamycin injection product monograph. Kirkland, Quebec; 28 August 2007.
BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 69/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
93. Schering Canada Inc. Caelyx Package Insert. Pointe-Claire, Quebec; September 2001.
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102. Berlex Canada Inc. Fludara Package Insert. Lachine, Quebec; December 1998.
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