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DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special
(Storage Prior to Use, With: Stability Precautions/Notes
Manufacturer, Preservative
Status)
Leucovorin
1 1,2
50 mg/5 mL N/A 10 mg/mL discard unused syringe 8 h RT
1
(GMP) portion
(F)(PFL)
1
no preservative 0.05-10 mg/mL NS, D5W, LR,
NS, D5W, Ringer’s, Ringer’s:
1,2 1
LR, D10W, D5NS 24 h RT
Leucovorin
3 3 3
50 mg/5 mL N/A 10 mg/mL 8h syringe 8 h RT
500 mg/50 mL
(Pfizer/Hospira)
(F)(PFL) 0.05 – 10 mg/mL NS, NS, D5W, LR,
3
no preservative D5W, LR, Ringer’s, Ringer’s:
3 3
D10W, D5NS 24 h RT
D5W:
4
12 h RT
D10NS:
4
6 h RT
Mesna
11
400 mg/4 mL N/A 100 mg/mL discard unused greater than 1 mg/mL complete
11
1000 mg/10 mL portion in D5W, D5½NS, NS, administration within
11-13 11
(Baxter) (use filter needle to LR 24 h RT
(RT) withdraw from
11
no preservative ampoule)
Mesna
11 11
1000 mg/10 mL N/A 100 mg/mL 8 days RT greater than 1 mg/mL complete
5000 mg/50 mL in D5W, D5½NS, NS, administration within
11-13 11
(Baxter) (vial may be LR 24 h RT
(RT) punctured up to 4
11 11
preservative times)
Mesna
14 14,15 14
1000 mg/10mL N/A 100 mg/mL 14 d RT,F greater than or equal 24 h RT, 48 h F
(Fresenius Kabi) to 1 mg/mL in NS or
16
(RT) D5W
14
preservative
Methotrexate
17 2
IT Injection N/A 25 mg/mL discard unused qs to 6 mL with use within 4 h of initial - auxiliary info
17 2
Only preservative free portion preservative free puncture - label to include
24,25
methotrexate may be NS route in full (i.e.,
administered by the INTRATHECAL
23
intrathecal route injection) attached
50 mg/2mL to both syringe and
26
(Accord) outer ziplock bag
(RT)(PFL)
17
no preservative
Methotrexate
27
50 mg/2mL N/A 25 mg/mL 50mg: syringe use within 8 h RT of - for high-dose
27
500 mg/20mL discard unused initial puncture regimens (e.g., 1-
27 2
1 g/40mL portion 12 g/m as a single
18-22
2.5 g/100 mL dose) : use
(Pfizer/Hospira) 500 mg, 1 g, or 0.4–2 mg/mL NS, use within 24 h RT of preservative-free
27 27 27
(RT)(PFL) 2.5 g: D5W initial puncture methotrexate
27 27
no preservative 8 h RT - do not use for IT
(100 mL* NS, D5W) **(PFL) injection
Methotrexate
27 15,27 15
50 mg/2mL N/A 25 mg/mL 14 d F syringe 14 d F - contains benzyl
27
500 mg/20mL alcohol
(Pfizer/Hospira) - do NOT use for
(RT)(PFL) 0.4–2 mg/mL NS, 24 h RT
27 high-dose
27
preservative D5W
27 regimens (e.g., 1-
2
12 g/m as a single
27
(100 mL* NS, D5W) dose)
- do NOT use for IT
27
injection
Mitomycin
28 28 28 28
20 mg 40 mL SWI 0.5 mg/mL 6 h RT, 72 h F syringe 6 h RT, 72 h F
(Accord)
28 28 28
(RT)(PFL) shake well **(PFL) **(PFL)
28
no preservative
Mitomycin
28 28 28 28
intraperitoneal 40 mL SWI 0.5 mg/mL 6 h RT, 72 h F 0.02-0.04 mg/mL NS:
28
20 mg 3 h RT, 18 h F
28 28 28
(Accord) shake well **(PFL) NS, sodium lactate
(RT)(PFL) sodium lactate:
28 28
no preservative 3 h RT, 6 h F
Mitomycin
32 32 32 32
20 mg 40 mL SWI 0.5 mg/mL 6 h RT, 72 h F syringe 6 h RT, 72 h F
(Teva/Novopharm)
32 32 32
(RT)(PFL) shake well **(PFL) **(PFL)
32
no preservative
Mitomycin
32 32 32 32
intraperitoneal 40 mL SWI 0.5 mg/mL 6 h RT, 72 h F 0.02-0.04 mg/mL NS:
32
20 mg 6 h RT, 18 h F
32 32 32
(Teva/Novopharm) shake well **(PFL) NS, sodium lactate
(RT)(PFL) sodium lactate:
32 32
no preservative 6 h RT, F
mitoXANTRONE
33 33 33
20 mg/10 mL N/A 2 mg/mL discard unused NS, D5W 24 h RT
33
(Fresenius Kabi) portion
(RT) Greater than or equal
33 33
no preservative to *50 mL
mitoXANTRONE
35 35
20 mg/10 mL N/A 2 mg/mL discard unused Greater than or equal 24 h RT
35 35
(Teva/Novopharm) portion to *50 mL NS, D5W
36
(RT)(PFL) **(PFL)
35
no preservative
Nivolumab
37
40 mg/4 mL N/A 10 mg/mL discard unused 1-10 mg/mL NS, complete - administer with a
37 37
100 mg/10 mL portion D5W administration within 0.2 to 1.2 micron
37 37
(BMS) 8 h RT or 24 h F in-line filter
(F)(PFL) (50-100* mL) - discard if cloudy
37
do not shake **(PFL) or has pronounced
37
no preservative mix by gentle colour change
inversion; do not (should be clear to
37 37
shake pale yellow)
Octreotide
41 41 41 41
50 mcg/mL N/A 50 mcg/mL Use within 4 h NS 24 h RT
100 mcg/mL
41
500 mcg/mL 100 mcg/mL volume adjusted to
(Omega) ensure a continuous
41
(F)(PFL) 500 mcg/mL infusion of octreotide
41 41
no preservative at 25 mcg/hour
Octreotide
41 41 41 41
multidose vial: N/A 200 mcg/mL 15 d F NS 24 h RT
1000 mcg/5 mL
(Omega) volume adjusted to
(F)(PFL) ensure a continuous
41
preservative infusion of octreotide
41
at 25 mcg/hour
Octreotide
42 42,43 42,43
multidose vial: N/A 200 mcg/mL 14 d F SC syringe use within 14 d F
1000 mcg/5 mL
(Teva/Novopharm)
42 42
(F)(PFL) infusion: NS 24 h RT
42
preservative
Octreotide
44 10,46,47 46
(SANDOSTATIN®) N/A 200 mcg/mL discard unused 50–200 mL NS 24 h RT
45
1000 mcg/5 mL portion
(Novartis) SC infusion: adjust
(F)(PFL) volume to ensure
44
preservative infusion rate of 25
46
mcg/h
Octreotide
(SANDOSTATIN LAR®) 2 mL supplied 10 mg: 5 mg/mL discard unused deep intragluteal use within 4 h of initial - do NOT shake
46 46 7,46
10 mg diluent portion administration only reconstitution
20 mg 20 mg: 10 mg/mL
30 mg gently run 2 mL
46
(Novartis) down sides of the 30 mg: 15 mg/mL
(F)(PFL) vial; do NOT disturb
45
no preservative for 2–5 min, then
46
swirl moderately
record time of
reconstitution
Olaratumab
49 49
500 mg/50 mL N/A 10 mg/mL discard unused dilute to a final complete - do NOT shake
39,49
(Lilly) portion volume of 250 mL administration within
49
(F)(PFL) NS 24 h F, plus an
49
do not shake additional 12 h RT
49
no preservative do NOT use D5W or
other dextrose
49
containing solutions
49
gently invert to mix
Oxaliplatin
51 39,53 51
50 mg/10 mL N/A 5 mg/mL 2 d F, RT 0.2-0.7 mg/mL 0.2-2 mg/mL:
51
100 mg/20 mL 24 h RT, 48 h F
51
150 mg/30 mL 250-500 mL D5W
200 mg/40 mL
(Sandoz) do NOT use NS or
(RT)(PFL) other chloride-
51 51
no preservative containing solution
do NOT use
aluminum-containing
51
needle and syringe
do NOT use
aluminum-containing
54
needle and syringe
PACLitaxel
55
30 mg/5 mL N/A 6 mg/ mL 30 mg: 0.3-1.2 mg/mL in NS, complete - use non-DEHP
39,55 55
100 mg/16.7 mL 48 h RT D5W, D5NS, D5LR administration within bag and tubing with
55
300 mg/50 mL 27 h RT 0.22 micron in-line
55
(Accord) 100 mg: (e.g., 100-1000 mL)* filter
39,55
(RT)(PFL) 48 h RT - avoid excessive
55 55
no preservative shaking
300 mg:
55
24 h RT
59
0.012-0.12 mg/mL in 16 h RT
61
NS
PACLitaxel
64 39,64,65
30 mg/5 mL N/A 6 mg/mL 48 h RT 0.3-1.2 mg/mL in NS, complete - use non-DEHP
64
100 mg/16.7 mL D5W, D5NS, D5LR administration within bag and tubing with
64
150 mg/25 mL 27 h RT 0.22 micron in-line
64
300 mg/50 mL (e.g., 100-1000 mL)* filter
(Hospira)
(RT)(PFL)
63
preservative
Pamidronate
70 70
30 mg/10 mL N/A 3 mg/mL discard unused Less than or equal to 24 h RT - do NOT mix with
70 70
60 mg/10 mL portion 0.36 mg/mL NS, calcium containing
70 70
90 mg/10 mL D5W solutions
70
(Fresenius Kabi) 6 mg/mL
(RT)
70
no preservative
70
9 mg/mL
Pamidronate
72 72
30 mg/10 mL N/A 3 mg/mL discard unused 0.06–0.36 mg/mL in 24 h F followed by 24 h - do NOT mix with
72 72 72
60 mg/10 mL portion NS, D5W RT (total 48 h) calcium containing
90 mg/10 mL solution (e.g.,
72 72 72
(Omega) 6 mg/mL **(PFL) Ringer’s)
(RT)
72
no preservative
72
9 mg/mL
Pamidronate
73
30 mg/10 mL N/A 3 mg/mL discard unused 0.06-0.36 mg/mL in 24 h F followed by 24 h - do NOT mix with
73 73 73
60 mg/10 mL portion NS, D5W RT (total 48 h) calcium containing
90 mg/10 mL solution (e.g.,
73 73 73
(Pfizer) 6 mg/mL **(PFL) Ringer’s)
(RT)
73
no preservative
73
9 mg/mL
PANitumumab
75 75,76
100 mg/5 mL N/A 20 mg/mL discard unused Less than or equal to 24 h F, 6 h RT - administer with
75
400 mg/20 mL portion 1000 mg: 0.2 or 0.22 micron
75 75
(Amgen) 100 mL NS in-line filter
(F)(PFL) - solution may
do not shake Greater than 1000mg: contain particulates
75 75
no preservative 150 mL NS which do not affect
75
product quality
75,76
1-10mg/mL - do not administer
75
if discoloured
IV: bag:
77
100 mL NS, D5W use within 4 h of vial
39,77
puncture
Pembrolizumab
78
100 mg/4 mL N/A 25 mg/mL discard unused 1-10 mg/mL complete - use a 0.2 to 5
39,78 78
(Merck) portion NS, D5W administration within micron in-line
78 78
(F)(PFL) 6 h RT, 24 h F filter
do not shake mix by gentle - allow vials and
78 78
no preservatives inversion diluted solutions to
come to RT prior to
78
use
- vials contain 0.25
78
mL overfill
Pemetrexed
80 80 80
100 mg 100 mg: 25 mg/mL 24 h F, RT 100 mL 24 h F, RT - do NOT mix with
80 80
500 mg 4.2 mL NS NS calcium containing
(Accord) solution (e.g.,
80
(RT) 500 mg: Ringer’s)
80 80
no preservative 20 mL NS
Pemetrexed
81 81 81
100 mg 100 mg: 25 mg/mL 24 h F, RT 100 mL 24 h F, RT - do NOT mix with
81 81
500 mg 4.2 mL NS NS calcium containing
(Eli Lilly) solution (e.g.,
82
(RT) 500 mg: Ringer’s)
81
no preservative 20 mL preservative-
81
free NS
Plerixafor
84 84 43,85
24 mg/1.2 mL N/A 20 mg/mL discard unused SC syringe 48 hours RT
84
(sanofi-aventis) portion
(RT)
84
no preservative
Porfimer
86 86
15 mg 15 mg: 2.5 mg/mL 24 h F syringe use within 4 h of initial - avoid contact with
86 7,87
75 mg 6.6 mL D5W reconstitution skin and eyes;
86
(Axcan) **(PFL) protect exposed
86 86
(RT)(PFL) 75 mg: **(PFL) area from light
86 86
no preservative 31.8 mL D5W
record time of
reconstitution
Raltitrexed
88 88 88
2 mg 4 mL SWI 0.5 mg/mL 24 h F, RT 50-250 mL NS, complete
88
(Pfizer) D5W administration within
88
(F,RT)(PFL) 24 h F, RT
88
(no preservative)
riTUXimab
91 92,93
100 mg/10 mL N/A 10 mg/mL discard unused 1-4 mg/mL NS, 24 h F, 12 h RT - once removed
91 91
500 mg/50 mL portion D5W from the fridge,
(Roche) compounded
(F)(PFL) (e.g., 250-500 mL)* product is stable
91 92,93
no preservative for 12h RT
riTUXimab
94 94 94
subcutaneous N/A 120 mg/mL discard unused SC syringe 48 h F plus 8 h RT - contains
94 94
1400 mg/11.7 mL portion hyaluronidase
1600 mg/13.4 mL - formulations are
(Roche) NOT
94
(F)(PFL) interchangeable
94
no preservative
Siltuximab
98 98 98
100 mg 100 mg: 20 mg/mL 2 h RT 250 mL D5W complete - use 0.2 micron in-
98 98
400 mg 5.2 mL SWI administration within line filter
98
(Janssen) dilute to 250 mL final 6 h RT
(F)(PFL) 400 mg: volume by
98 98
no preservative 20 mL SWI withdrawing volume
from bag equal to
allow vial to come to volume of drug to be
98
room temperature added
prior to use (~30
98
minutes)
Temsirolimus
100,101 100,101 100,101
30 mg/1.2 mL 1.8 mL supplied 10 mg/mL 24 h RT 250 mL NS complete - use non-DEHP
100,101
(Wyeth) diluent administration within 6 bag and tubing with
100,101 100 100,101 100,101
(F)(PFL) **(PFL) h in-line filter
102
no preservative
Teniposide
103
50 mg/5 mL N/A 10 mg/mL discard unused 50 – 500 mL NS or 0.1-0.4 mg/mL: 24 h - do not refrigerate
103
(BMS) portion D5W for a final RT - use non-DEHP
103
(RT) concentration of 0.1-1 bag and tubing
103 103
preservative mg/mL 1 mg/mL: complete - do not use if
103,104
administration within 4 precipitates
h of preparation - contains DMA***
103,104
RT - excessive
agitation may
cause
103
precipitation
record time of
reconstitution
Thyrotropin alfa
108 108 108 108 108
1.1 mg 1.2 mL SWI 0.9 mg/mL 24 h F syringe 24 h F
(Genzyme)
108
(F)(PFL) swirl contents
108
no preservative
do NOT shake
Topotecan
110 2,110
4 mg/4 mL N/A 1 mg/mL discard unused 0.025-0.5 mg/mL 14 d F, 48 h RT
2,110
(Accord) portion
(RT)(PFL) 50-100 mL NS,
110 110
no preservative D5W
Topotecan
111 111 111
1 mg 1 mg: 1 mg/mL 24 h F,RT 0.02-0.5 mg/mL 24 F, RT
111
4 mg 1.1 mL SWI
(Actavis) 50-100 mL NS,
111
(RT)(PFL) 4 mg: D5W
111 111
no preservative 4 mL SWI
Topotecan
112 112
4 mg/4 mL N/A 1 mg/mL discard unused 0.02-0.5 mg/mL 24 h F, RT
2,112
(Pfizer/Hospira) portion
(F)(PFL) 50-100 mL NS,
112 112
no preservative D5W
Trastuzumab
114 39 114 114 114
(HERCEPTIN®) 20 mL supplied 21 mg/mL 14 d F 250 mL NS only 24 h F, RT - do NOT shake
114
440 mg BWI
(Roche) do NOT use dextrose
114
(F) swirl vial gently; containing solutions
114
preservative allow to stand
undisturbed for 5
114
min
Treosulfan
118 7,118 119 7,118
1g pre-heat SWI to 50 mg/mL 48 h RT undiluted 48 h RT - compatible with
5g 30°C (not higher) polytetrafluoroethyl
118
(medac) shake vial carefully dilute with NS or D5W ene filters
(RT) before adding the in empty infusion bag - may require
118
no preservative warmed SWI for final concentration vigorous shaking to
118 118
1 g vial: 20 mL SWI, = 20 mg/mL reconstitute
while slightly
shaking vial and
syringe; continue
shaking the
reconstituted
solution for another
118
2 min
5 g vial: 100 mL
SWI, while slightly
shaking vial and
syringe; continue
shaking the
reconstituted
solution for another
118
2 min
vinBLAStine
126
10 mg/10 mL N/A 1 mg/mL discard unused 25-50 mL NS, use within 4 h of initial - auxiliary info:
126 121,127 39
(Teva) portion D5W puncture WARNING: FOR
(F)(PFL) INTRAVENOUS
126
no preservative USE ONLY –
FATAL IF GIVEN
BY OTHER
124,125
ROUTES
Vinorelbine
131 131 131
10 mg/1 mL N/A 10 mg/mL discard unused 0.5-2.0 mg/mL 24 h F, RT - auxiliary info:
131
50 mg/5mL portion WARNING: FOR
(Fresenius Kabi) NS, D5W, ½NS, INTRAVENOUS
(F)(PFL) D5½NS, Ringer’s, USE ONLY –
131 131
no preservative Ringer’s Lactate FATAL IF GIVEN
BY OTHER
124,132
ROUTES
Vinorelbine
134 134 134
10 mg/1 mL N/A 10 mg/mL discard unused 0.5–2.0 mg/mL 24 h F, RT - auxiliary info:
134
50 mg/5 mL portion WARNING: FOR
(Pfizer/Hospira) 50 mL* NS, D5W, INTRAVENOUS
(F)(PFL) ½NS, D5½NS, USE ONLY –
134
no preservative Ringer’s, Ringer’s FATAL IF GIVEN
134
Lactate BY OTHER
124,132
ROUTES
Vinorelbine
135 135 135
10 mg/1 mL N/A 10 mg/mL discard unused 0.5–2.0 mg/mL 24 h F, RT - auxiliary info:
135
50 mg/5 mL portion WARNING: FOR
(Teva) 50 mL* NS, D5W, INTRAVENOUS
(F)(PFL) ½NS, D5½NS, USE ONLY –
135
no preservative Ringer’s, Ringer’s FATAL IF GIVEN
135
Lactate BY OTHER
124,132
ROUTES
Zoledronic acid
137 137
4 mg/5 mL N/A 0.8 mg/mL discard unused 100 mL NS, D5W complete infusion - do NOT mix with
137
(Marcan) portion within 24 h of calcium containing
137
(RT) preparation solutions (e.g.,
137
no preservative Lactated
137
Refrigerate diluted Ringer’s)
product if not used
immediately after
preparation; bring to
RT prior to
137
administration
Zoledronic acid
139 139
(ZOMETA) N/A 0.8 mg/mL discard unused 100 mL NS, D5W complete infusion - do NOT mix with
39
4 mg/ 5 mL portion within 24 h of calcium containing
139 139
(Novartis) preparation solutions
(RT)
139
no preservative Refrigerate diluted
product if not used
immediately after
preparation; bring to
RT prior to
139
administration
* 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.
*** Contains DMA (N,N dimethylacetamide). Product may be incompatible with closed system transfer devices such as ChemoLock.
Centres are not to change the content locally but should forward suggestions to the Cancer Drug Manual staff.
Explanatory Notes
Stability data assumes products prepared using standard aseptic technique in biological safety cabinet at low risk for contamination according to the classification
141,142
outlined in USP 797.
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 fridge stability is bolded as preferred (ie, to minimize
growth of micro-organisms).
Discard unused portion: Unused portion from single use vials should be discarded at the end of the day.
“overfill known” is stated if the manufacturer states overfill that is present is within acceptable limits.
“Complete administration within __” is stated if the manufacturer specifies that the infusion must be completed in a specific time frame following preparation,
usually including entire time required for preparation (from first puncture), storage, and administration of infusion.
References
1. Generic Medical Partners Inc. Leucovorin calcium injection product monograph. Toronto, Ontario; 13 August 2018.
2. BC Cancer. Provincial Pharmacy Directive Number II-20: Chemotherapy Preparation Chart. Vancouver, British Columbia: BC Cancer; 5 December 2018.
3. Pfizer Canada Inc. Leucovorin calcium injection product monograph. Kirkland, Quebec; 21 June 2018.
4. Teva Canada Limited. Leucovorin calcium injection® product monograph. Toronto, Ontario; 5 May 2014.
5. Hospira Healthcare Corporation. LEUCOVORIN CALCIUM INJECTION® product monograph. Saint-Laurent, Quebec; 7 June 2007.
6. Novopharm Limited (Teva). LEUCOVORIN CALCIUM® Injection product information package. Toronto, Ontario; undated.
7. BC Cancer Agency. Pharmacy Policy Number II-20: Guiding Principles for Chemotherapy Preparation Chart. Vancouver, British Columbia: BC Cancer Agency; 6 January 2006.
8. Jenny Yeung. Personal communication. Medical Information Specialist, Teva Canada; 12 April 2017.
9. GlaxoSmithKline Inc. Alkeran Package Insert. Mississauga, Ontario; Montreal, Quebec; 2004.
10. Trissel LA. Handbook on Injectable Drugs. 13th ed. Bethesda, MD: American Society of Health-System Pharmacists, Inc.; 2005.
11. Baxter Corporation. UROMITEXAN® product monograph. Mississauga, Ontario; 6 August 2013.
12. Mona Ghobros BPharm MSc. Personal communication. Medical Information, Baxter Corporation; 29 November 2018.
13. Trissel's® 2 Clinical Pharmaceutics Database (database on the Internet). Mesna. Lexi-Comp Inc.; created by Lawrence A. Trissel, Available at: http://online.lexi.com. Accessed 29
November 2018.
14. Fresenius Kabi Canada Ltd. Mesna for injection product monograph. Richmond Hill, Ontario; 21 December 2017.
15. BC Cancer. Pharmacy Policy Number II-20: Guiding Principles for Chemotherapy Preparation Chart. Vancouver, British Columbia: BC Cancer; 19 September 2007.
16. Fresenius Kabi Canada Ltd. Mesna for injection product monograph. Richmond Hill, Ontario; 30 March 2015.
17. Accord Healthcare Inc. Methotrexate injection product monograph. Kirkland, Quebec; 6 April 2018.
18. BC Cancer Agency Miscellaneous Origins Tumour Group. (MOHDMTX) BCCA Protocol Summary for Treatment of Meningeal Disease (Miscellaneous Tumour Origins) using High
Dose Methotrexate with Leucovorin Rescue. Vancouver, British Columbia: BC Cancer Agency; 1 Jan 2013.
19. BC Cancer Agency Sarcoma Tumour Group. (SAHDMTX) BCCA Protocol Summary for Treatment of Osteosarcoma Using High Dose Methotrexate with Leucovorin Rescue.
Vancouver, British Columbia: BC Cancer Agency; 1 Nov 2012.
20. BC Cancer Agency Lymphoma Tumour Group. (LYHDMRP) BCCA Protocol Summary for Treatment of Primary Intracerebral Lymphoma with High Dose Methotrexate and
riTUXimab. Vancouver, British Columbia: BC Cancer Agency; 1 Jun 2014.
21. BC Cancer Agency Lymphoma Tumour Group. (LYHDMTXP) BCCA Protocol Summary for Treatment of Primary Intracerebral Lymphoma with High Dose Methotrexate.
Vancouver, British Columbia: BC Cancer Agency; 1 Jun 2014.
22. BC Cancer Agency Lymphoma Tumour Group. (LYHDMTXR) BCCA Protocol Summary for Treatment of Leptomeningeal Lymphoma or Recurrent Intracerebral Lymphoma with
High Dose Methotrexate. Vancouver, British Columbia: BC Cancer Agency; 1 Jun 2014.
23. Mayne Pharma Canada. Methotrexate Product Monograph. Montreal, Quebec; December 2003.