(protamine zinc recombinant
human insulin)
Caution:
Federal law restricts this drug to use by or on the order of a licensed
veterinarian.
Description:
ProZinc™ insulin is a sterile aqueous protamine zinc suspension of
recombinant human insulin.
Each mL contains:
|
recombinant human
insulin |
40 International
Units (IU) |
|
protamine sulfate |
.466 mg |
|
zinc oxide |
0.088 mg |
|
glycerin |
16.00 mg |
|
dibasic sodium
phosphate, heptahydrate |
3.78 mg |
|
phenol (added as
preservative) |
2.50 mg |
|
hydrochloric acid |
1.63 mg |
|
water for injection
(maximum) |
1005 mg |
pH is adjusted with
hydrochloric acid and/or sodium hydroxide.
Indications: ProZinc (protamine zinc recombinant human insulin) is
indicated for the reduction of hyperglycemia and hyperglycemia-associated
clinical signs in cats with diabetes mellitus.
Dosage and
Administration: USE OF A SYRINGE OTHER THAN A U-40 SYRINGE WILL RESULT
IN INCORRECT DOSING.
FOR SUBCUTANEOUS INJECTION IN
CATS ONLY.
ProZinc insulin should be
mixed by gently rolling the vial prior to withdrawing each dose from the
vial. Using a U-40 insulin syringe, the injection should be administered
subcutaneously on the back of the neck or on the side of the cat.
Always provide the Cat
Owner Information Sheet with each prescription. The initial recommended
ProZinc dose is 0.1 - 0.3 IU insulin/pound of body weight (0.2 - 0.7 IU/kg)
every 12 hours. The dose should be given concurrently with or right after a
meal. The veterinarian should re-evaluate the cat at appropriate intervals
and adjust the dose based on both clinical signs and glucose nadirs until
adequate glycemic control has been attained. In the effectiveness field
study, glycemic control was considered adequate if the glucose nadir from a
9-hour blood glucose curve was between 80 and 150 mg/dL and clinical signs
of hyperglycemia such as polyuria, polydipsia, and weight loss were
improved.
Further adjustments in the
dosage may be necessary with changes in the cat’s diet, body weight, or
concomitant medication, or if the cat develops concurrent infection,
inflammation, neoplasia, or an additional endocrine or other medical
disorder.
Contraindications: ProZinc insulin is contraindicated in cats sensitive
to protamine zinc recombinant human insulin or any other ingredients in the
ProZinc product. ProZinc insulin is contraindicated during episodes of
hypoglycemia.
Warnings: User
Safety: For use in cats only. Keep out of the reach of children. Avoid
contact with eyes. In case of contact, immediately flush eyes with running
water for at least 15 minutes. Accidental injection may cause hypoglycemia.
In case of accidental injection, seek medical attention immediately.
Exposure to product may induce a local or systemic allergic reaction in
sensitized individuals.
Animal Safety:
Owners should be advised to observe for signs of hypoglycemia (see Cat Owner
Information Sheet). Use of this product, even at established doses, has been
associated with hypoglycemia. An animal with signs of hypoglycemia should be
treated immediately. Glucose should be given orally or intravenously as
dictated by clinical signs. Insulin should be temporarily withheld and, if
indicated, the dosage adjusted.
Any change in insulin should
be made cautiously and only under a veterinarian’s supervision. Changes in
insulin strength, manufacturer, type, species (human, animal) or method of
manufacture (rDNA versus animal-source insulin) may result in the need for a
change in dosage.
Appropriate diagnostic tests
should be performed to rule out other endocrinopathies in diabetic cats that
are difficult to regulate.
Precautions:
Animals presenting with severe ketoacidosis, anorexia, lethargy, and/or
vomiting should be stabilized with short-acting insulin and appropriate
supportive therapy until their condition is stabilized. As with all insulin
products, careful patient monitoring for hypoglycemia and hyperglycemia are
essential to attain and maintain adequate glycemic control and to prevent
associated complications. Overdosage can result in profound hypoglycemia and
death. Progestogens, certain endocrinopathies and glucocorticoids can have
an antagonistic effect on insulin activity. Progestogen and glucocorticoid
use should be avoided.
Reproductive
Safety: The safety and effectiveness of ProZinc insulin in breeding,
pregnant, and lactating cats has not been evaluated.
Use in
Kittens: The safety and effectiveness of ProZinc insulin in kittens has
not been evaluated.
Adverse
Reactions: Effectiveness Field Study
In a
45-day effectiveness field study, 176 cats received ProZinc insulin.
Hypoglycemia (defined as a blood glucose value of < 50 mg/dL) occurred in 71
of the cats at various times throughout the study. Clinical signs of
hypoglycemia were generally mild in nature (described as lethargic,
sluggish, weak, trembling, uncoordinated, groggy, glassy-eyed or dazed). In
17 cases, the veterinarian provided oral glucose supplementation or food as
treatment. Most cases were not associated with clinical signs and received
no treatment. One cat had a serious hypoglycemic event associated with
stupor, lateral recumbency, hypothermia and seizures. All cases of
hypoglycemia resolved with appropriate therapy and if needed, a dose
reduction.
Three cats had injection site
reactions which were described as either small, punctate, red lesions;
lesions on neck; or palpable subcutaneous thickening. All injection site
reactions resolved without cessation of therapy.
Four cats developed diabetic
neuropathy during the study as evidenced by plantigrade stance. Three cats
entered the study with plantigrade stance, one of which resolved by Day 45.
Four cats were diagnosed with diabetic ketoacidosis during the study. Two
were euthanized due to poor response to treatment. Five other cats were
euthanized during the study, one of which had hypoglycemia. Four cats had
received ProZinc insulin for less than a week and were euthanized due to
worsening concurrent medical conditions.
The following additional
clinical observations or diagnoses were reported in cats during the
effectiveness field study: vomiting, lethargy, diarrhea, cystitis/hematuria,
upper respiratory infection, dry coat, hair loss, ocular discharge, abnormal
vocalization, black stool, and rapid breathing.
Extended
Use Field Study
Cats that
completed the effectiveness study were enrolled into an extended use field
study. In this study, 145 cats received ProZinc insulin for up to an
additional 136 days. Adverse reactions were similar to those reported during
the 45-day effectiveness study and are listed in order of decreasing
frequency: vomiting, hypoglycemia, anorexia/poor appetite, diarrhea,
lethargy, cystitis/hematuria, and weakness. Twenty cats had signs consistent
with hypoglycemia described as: sluggish, lethargic, unsteady, wobbly,
seizures, trembling, or dazed. Most of these were treated by the owner or
veterinarian with oral glucose supplementation or food; others received
intravenous glucose. One cat had a serious hypoglycemic event associated
with seizures and blindness. The cat fully recovered after supportive
therapy and finished the study. All cases of hypoglycemia resolved with
appropriate
therapy and if needed, a dose
reduction.
Fourteen cats died or were
euthanized during the extended use study. In two cases, continued use of
insulin despite anorexia and signs of hypoglycemia contributed to the
deaths. In one case, the owner decided not to continue therapy after a
presumed episode of hypoglycemia. The rest were due to concurrent medical
conditions or worsening of the diabetes mellitus.
To report suspected adverse
reactions, or to obtain a copy of the Material Safety Data Sheet (MSDS),
call 1-866-638-2226.
Information
for Cat Owners: Please refer to the Cat Owner Information Sheet for more
information about ProZinc insulin. ProZinc insulin, like other insulin
products, is not free from adverse reactions. Owners should be advised of
the potential for adverse reactions and be informed of the associated
clinical signs. Potential adverse reactions include: hypoglycemia, insulin
antagonism/resistance, rapid insulin metabolism, insulin-induced
hyperglycemia (Somogyi Effect), and local or systemic reactions. The most
common adverse reaction observed is hypoglycemia. Signs may include:
weakness, depression, behavioral changes, muscle twitching, and anxiety. In
severe cases of hypoglycemia, seizures and coma can occur.
Hypoglycemia can be fatal if
an affected cat does not receive prompt treatment. Appropriate veterinary
monitoring of blood glucose, adjustment of insulin dose and regimen as
needed, and stabilization of diet and activity help minimize the risk of
hypoglycemic episodes. The attending veterinarian should evaluate other
adverse reactions on a case-by-case basis to determine if an adjustment in
therapy is appropriate, or if alternative therapy should be considered.
Effectiveness:
A total of 187 client-owned cats were enrolled in a 45-day field study, with
176 receiving ProZinc insulin. One hundred and fifty-one cats were included
in the effectiveness analysis. The patients included various purebred and
mixed breed cats ranging in age from 3 to 19 years and in weight from 4.6 to
20.8 pounds. Of the cats included in the effectiveness analysis, 101 were
castrated males, 49 were spayed females, and 1 was an intact female.
Cats were started on ProZinc
insulin at a dose of 0.1-0.3 IU/lb (0.2-0.7 IU/kg) twice daily. Cats were
evaluated at 7, 14, 30, and 45 days after initiation of therapy and the dose
was adjusted based on clinical signs and results of 9-hour blood glucose
curves on Days 7, 14, and 30.
Effectiveness was based on
successful control of diabetes which was defined as improvement in at least
one blood glucose variable (glucose curve mean, nadir, or fructosamine) and
at least one clinical sign (polyuria, polydipsia, or body weight). Based on
this definition, 115 of 151 cases (76.2%) were considered successful. Blood
glucose curve means decreased from 415.3 mg/dL on Day 0 to 203.2 mg/dL by
Day 45 and the mean blood glucose nadir decreased from 407.9 mg/dL on Day 0
to 142.4 mg/dL on Day 45. Mean fructosamine values decreased from 505.9
µmol/L on Day 0 to 380.7 µmol/L on Day 45.
Cats that completed the
effectiveness study were enrolled in an extended use field study. The mean
fructosamine value was 342.0 µmol/L after a total of 181 days of ProZinc
therapy.
How Supplied:
ProZinc insulin is supplied as a sterile injectable suspension in 10 mL
multidose vials. Each mL of ProZinc product contains 40 IU recombinant human
insulin.
Storage
Conditions: Store in an upright position under refrigeration at 36-46°F
(2-8°C). Do not freeze. Protect from light.