Zoetis Cerenia Handleiding

Zoetis Niet gecategoriseerd Cerenia

Lees hieronder de 📖 handleiding in het Nederlandse voor Zoetis Cerenia (3 pagina's) in de categorie Niet gecategoriseerd. Deze handleiding was nuttig voor 17 personen en werd door 2 gebruikers gemiddeld met 4.5 sterren beoordeeld

Pagina 1/3

Tablets and Injectable Solution

Antiemetic

CERENIA Tablets

For oral use in dogs only

CERENIA Injectable

For subcutaneous or intravenous injection in dogs and cats

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

DESCRIPTION: Maropitant is a neurokinin (NK 1

) receptor antagonist that blocks the pharmacological action of substance P in the central

nervous system (CNS). Maropitant is the non-proprietary designation for a substituted quinuclidine. The empirical formula is C

32H40N2O

C6H8O7H2O and the molecular weight 678.81. The chemical name is (2 -butyl-2-methoxybenzyl) quinuclidin-S S N tert,3 )-2-benzhydryl- -(5-

3-amine citrate monohydrate. Each peach-colored oval tablet is scored and contains 16, 24, 60or 160mg of maropitant as maropitant

citrate per tablet. Each mL of CERENIA Injectable Solution contains 10 mg maropitant, 63 mg sulphobutylether-beta-cyclodextrin, 3.3 mg

meta-cresol and water for injection.

The chemical structure of maropitant citrate is:

INDICATIONS: CERENIA (maropitant citrate) Tablets are indicated for the prevention of acute vomiting and the prevention of vomiting due to

motion sickness in dogs. CERENIA (maropitant citrate) Injectable Solution is indicated for the prevention and treatment of acute vomiting in

dogs and for the treatment of vomiting in cats.

DOSAGE AND ADMINISTRATION (CERENIA Tablets):

For Prevention of Acute Vomiting:

For Prevention of Acute Vomiting in dogs 2-7 months of age: Administer CERENIA Tablets orally at a minimum dose of 2 mg/kg

(0.9 mg/lb) body weight once daily for up to 5 consecutive days (see WARNINGS and Animal Safety).

For Prevention of Acute Vomiting in dogs 7 months of age and older: Administer CERENIA Tablets orally at a minimum dose of 2 mg/kg

(0.9 mg/lb) body weight once daily until resolution of acute vomiting.

If vomiting persists despite treatment, the case should be re-evaluated. CERENIA is most effective in preventing acute vomiting associated

with chemotherapy if administered prior to the chemotherapeutic agent.

For prevention of acute vomiting, dispense whole or half tablets in strength(s) that most closely result in a 2 mg/kg dose:

Dog body weight Number of Tablets

Pounds Kilograms 16 mg 24 mg 60 mg

8 4 1/2  

15 8 1  

25 12  1 

50 24  2 

65 30   1

130 60   2

Interchangeable use with CERENIA Injectable Solution for Prevention of Acute Vomiting:

In dogs that are actively vomiting, to ensure that the full initial dose is administered, CERENIA Injectable Solution is recommended at a

dose of 1 mg/kg once daily. Thereafter, for the prevention of acute vomiting, may be CERENIA Tablets at a dose of 2 mg/kg once daily

used interchangeably with CERENIA Injectable Solution for up to 5 days.

For Prevention of Vomiting Due to Motion Sickness in dogs 4 months and older:

Administer CERENIA Tablets orally at a minimum dose of 8 mg/kg (3.6 mg/lb) body weight once daily for up to 2 consecutive days

(see WARNINGS and Animal Safety).

Administer CERENIA Tablets a minimum of two hours prior to travel with a small amount of food to mitigate vomiting associated with

administration of the dose on an empty stomach; however, refrain from feeding a full meal prior to travel.

Prevention of Vomiting Due to Motion Sickness in Dogs 4 months of age and older:

Dispense whole or half tablets in strengths that most closely result in an 8 mg/kg dose once daily for up to 2 consecutive days:

Dog body weight Number of Tablets

Pounds Kilograms 16 mg 24 mg 60 mg 160 mg

2 1 1/2   

3 1.5  1/2  

4 2 1   

6 3  1  

8 4 2   

13 6  2  

16 7.5   1 

22 10    1/2

33 15   2 

44 20    1

66 30    1 1/2

88 40    2

132 60    3

CERENIA Injectable Solution should not be used interchangeably with CERENIA Tablets for the prevention of vomiting due to motion

sickness (8mg/kg).

DOSAGE AND ADMINISTRATION (CERENIA Injectable):

Use of refrigerated product may reduce the pain response associated with subcutaneous injection.

Dogs:

For Prevention and Treatment of Acute Vomiting in Dogs:

Dogs 2-4 Months of Age: Administer CERENIA Injectable Solution subcutaneously at 1 mg/kg (0.45 mg/lb) equal to 0.1 mL/kg (0.1 mL/2.2 lb)

of body weight once daily for up to 5 consecutive days.

Dogs 4 months of Age and Older: Administer CERENIA Injectable Solution intravenously over 1-2 minutes or subcutaneously at 1 mg/kg

(0.45 mg/lb) equal to 0.1 mL/1 kg (1 mL/22 lb) of body weight once daily for up to 5 consecutive days.

In dogs that are actively vomiting, it is recommended to initiate treatment with CERENIA Injectable Solution. Thereafter, CERENIA Tablets may

be used for the prevention of acute vomiting at 2 mg/kg once daily. (See CERENIA Tablets package insert for complete prescribing information).

For Prevention of Vomiting in Dogs 4 months of Age and Older Caused by Emetogenic Medications or Chemotherapeutic Agents:

Administer CERENIA Injectable Solution intravenously over 1-2 minutes or subcutaneously at 1 mg/kg (0.45 mg/lb) of body weight one time,

45-60 minutes prior to use of emetogenic medications or chemotherapeutic agents.

Cats:

For Treatment of Vomiting in Cats 4 Months of Age and Older:

Administer CERENIA Injectable Solution intravenously over 1-2 minutes or subcutaneously at 1 mg/kg (0.45 mg/lb) equal to 0.1 mL/kg

(0.1 mL/2.2 lb) of body weight once daily for up to 5 consecutive days.

The underlying cause of acute vomiting should be identiﬁed and addressed in dogs and cats that receive CERENIA Injectable Solution.

If vomiting persists despite treatment, the case should be re-evaluated.

WARNINGS: Not for use in humans. Keep out of the reach of children. In case of accidental ingestion, injection, or exposure, seek medical

advice. Topical exposure may elicit localized allergic skin reactions in some individuals. Repeated or prolonged exposure may lead to skin

sensitization. Wash hands with soap and water after administering drug and in case of accidental skin exposure. CERENIA is also an ocular

irritant. In case of accidental eye exposure, flush with water for 15minutes and seek medical attention.

In puppies younger than 11weeks of age, histological evidence of bone marrow hypocellularity was observed at higher frequency and greater

severity in puppies treated with CERENIA compared to control puppies. In puppies 16weeks and older, bone marrow hypocellularity was not

observed (see ).ANIMAL SAFETY

PRECAUTIONS: The safe use of CERENIA Tablets and Injectable Solution has not been evaluated in dogs or cats used for breeding, or in pregnant

or lactating bitches or queens.

The safe use of CERENIA Injectable Solution has not been evaluated in dogs or cats with gastrointestinal obstruction or that have ingested toxins.

Use with caution in patients with hepatic dysfunction because CERENIA Injectable Solution is metabolized by CYP3A, CYP2D15 (dogs) and

CYP1A (cats) enzymes (see ). The inﬂuence of concomitant drugs that may inhibit the metabolism of CERENIA Injectable Pharmacokinetics

Solution has not been evaluated. CERENIA Injectable Solution is highly protein bound. Use with caution with other medications that are highly

protein bound. The concomitant use of CERENIA Injectable Solution with other protein bound drugs has not been studied in dogs or cats.

Commonly used protein bound drugs include NSAIDs, cardiac, anticonvulsant, and behavioral medications. Drug compatibility should be

monitored in patients requiring adjunctive therapy.

CERENIA Tablets causes dose related decreases in appetite and body weight (see ). To maximize therapeutic potential of ANIMAL SAFETY

CERENIA Tablets, the underlying cause of vomiting should be identiﬁed and addressed in dogs receiving CERENIA Tablets.

ADVERSE REACTIONS:

CERENIA Tablets

Prevention of Acute Vomiting (minimum of 2mg/kg)

The following adverse reactions were reported during the course of a US field study for the prevention of acute vomiting in dogs treated with

CERENIA Tablets at a minimum of 2mg/kg orally and/or Injectable Solution at 1 mg/kg subcutaneously once daily for up to 5consecutive days:

Frequency of Adverse Reactions by Treatment

Adverse Reaction Placebo (n=69) CERENIA (n=206)

# dogs % occurrence # dogs % occurrence

Death during study 4 5.8 10 4.9

Euthanized during study 0 0 2 1

Diarrhea 6 8.7 8 3.9

Hematochezia/bloody stool 5 7.2 4 1.9

Anorexia 2 2.9 3 1.5

Otitis/Otorrhea 0 0 3 1.5

Endotoxic Shock 1 1.4 2 1

Hematuria 0 0 2 1

Excoriation 0 0 2 1

Other clinical signs were reported but were <0.5% of dogs.

Prevention of Vomiting Due to Motion Sickness (minimum of 8mg/kg)

The following adverse reactions were reported during US studies for the prevention of vomiting due to motion sickness in dogs treated with

CERENIA Tablets at a minimum of 8mg/kg orally one time. Dogs may have experienced more than one of the observed adverse reactions.

Frequency of Adverse Reactions by Treatment

Adverse Reaction

Placebo (n=195) CERENIA (n=208)

# dogs % occurrence # dogs % occurrence

Hypersalivation 19 9.7 26 12.5

Vomiting10 0 11 5.3

Muscle Tremors 1 0.5 2 1

Sedation/Depression 3 1.5 2 1

Retching 3 1.5 1 0.5

Flatulence 0 0 1 0.5

1Not associated with motion sickness

The following adverse reactions were reported during a European field study for the prevention of vomiting due to motion sickness in dogs

treated with CERENIA Tablets at a minimum of 8mg/kg orally once daily for 2consecutive days. Dogs may have experienced more than one

of the observed adverse reactions.

Frequency of Adverse Reactions by Treatment

Adverse Reaction Placebo (n=106) CERENIA (n=107)

# dogs % occurrence # dogs % occurrence

Vomiting 4 4 10 9

Drowsiness/Lethargy/Apathy 1 1 8 8

Hypersalivation 2 2 5 5

Anxiety 0 0 2 2

Trembling/Tremors 0 0 2 2

Inappetence 0 0 2 2

Mucus in stool 0 0 1 1

The following Adverse Reactions were reported during the conduct of a US clinical field trial where CERENIA Tablets were administered once

daily for 28 consecutive days to 32 dogs: lethargy, vomiting, inappetence, corneal edema, and enlarged lymph nodes.

Post-Approval Experience (Revised May 2019)

The following adverse events are based on post-approval adverse drug experience reporting. Not all adverse events are reported to FDA CVM.

It is not always possible to reliably estimate the adverse event frequency or establish a causal relationship to product exposure using these data.

The following adverse events reported for dogs are listed in decreasing order of frequency: anorexia, depression/lethargy, hypersalivation,

vomiting, diarrhea, trembling, ataxia, allergic reactions, weight loss, convulsion, hyperactivity, and panting.

Cases of ineffectiveness have been reported.

Cases of death (including euthanasia) have been reported.

To report suspected adverse events, for technical assistance or to obtain a copy of the SDS, contact Zoetis Inc. at 1-888-963-8471 or

www.zoetis.com.

For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or online at

www.fda.gov/reportanimalae.

ADVERSE REACTIONS:

CERENIA Injectable

DOGS:

In a US ﬁeld study for the prevention and treatment of vomiting associated with administration of cisplatin for cancer chemotherapy, the following

adverse reactions were reported in 77 dogs treated with CERENIA Injectable Solution at 1 mg/kg subcutaneously or 41 dogs treated with placebo:

Frequency of Adverse Reactions by Treatment

Adverse Reaction Placebo (n=41) CERENIA (n=77)

# dogs % occur # dogs % occur

Diarrhea 1 2.4 6 7.8

Anorexia 0 0 4 5.2

Injection site reaction

(swelling, pain upon injection) 0 0 3 4

Lethargy 1 2.4 2 2.6

The following adverse reactions were reported during the course of a US ﬁeld study for the prevention and treatment of acute vomiting in dogs

treated with 1 mg/kg CERENIA Injectable Solution subcutaneously and/or CERENIA Tablets at a minimum of 2 mg/kg orally once daily for up to

5 consecutive days:

Frequency of Adverse Reactions by Treatment

Adverse Reaction Placebo (n=69) CERENIA (n=206)

# dogs % occurrence # dogs % occurrence

Death during study 4 5.8 10 4.9

Euthanized during study 0 0 2 1

Diarrhea 6 8.7 8 3.9

Hematochezia/bloody stool 5 7.2 4 1.9

Anorexia 2 2.9 3 1.5

Otitis/Otorrhea 0 0 3 1.5

Endotoxic Shock 1 1.4 2 1

Hematuria 0 0 2 1

Excoriation 0 0 2 1

Other clinical signs were reported but were <0.5% of dogs.

Adverse reactions seen in a European ﬁeld study included ataxia, lethargy and injection site soreness in one dog treated with CERENIA

Injectable Solution.

Post-Approval Experience ( Rev. 2015)

The following adverse events are based on post-approval adverse drug experience reporting. Not all adverse events are reported to FDA CVM.

It is not always possible to reliably estimate the adverse event frequency or establish a causal relationship to product exposure using these data.

The following adverse events reported for dogs are listed in decreasing order of reporting frequency for CERENIA Injectable Solution:

Pain/vocalization upon injection, depression/lethargy, anorexia, anaphylaxis/anaphylactoid reactions (including swelling of the head/face),

ataxia, convulsions, hypersalivation, tremors, fever, dyspnea, collapse/loss of consciousness, recumbency, injection site reactions (swelling,

inﬂammation) and sedation.

Cases of death (including euthanasia) have been reported.

CATS ( :CERENIA Injectable Solution)

The following adverse reactions were reported during the course of a US ﬁeld study for the treatment of vomiting in cats treated with 1 mg/kg

CERENIA Injectable Solution subcutaneously once daily for up to ﬁve consecutive days:

Frequency of Adverse Reactions by Treatment

Adverse Reaction Placebo (n=62) CERENIA (n=133)

# cats % occurrence # cats % occurrence

Moderate Response to Injection

1,2 1 1.6 30 22.6

Signiﬁcant Response to Injection1,3 1 1.6 15 11.3

Fever/Pyrexia 2 3.2 2 1.5

Dehydration 0 0 3 2.3

Lethargy 0 0 2 1.5

Anorexia 0 0 1 0.8

Hematuria 0 0 1 0.8

Hypersalivation 0 0 1 0.8

Injection site swelling 1 1.6 0 0

The clinician observed and graded each cat’s response to injection.

Cat objected to the injection by retreating and vocalizing

Cat objected to the injection by retreating, hissing, scratching, and vocalization

Post-Approval Experience (Rev. 2015)

The following adverse events are based on post-approval adverse drug experience reporting. Not all adverse events are reported to FDA CVM.

It is not always possible to reliably estimate the adverse event frequency or establish a causal relationship to product exposure using these data.

The following adverse events reported for cats are listed in decreasing order of reporting frequency for CERENIA Injectable Solution: Depression/

lethargy, anorexia, hypersalivation, pain/ vocalization upon injection, dyspnea, ataxia, fever, recumbency, vomiting, panting, convulsion, and

muscle tremor.

Cases of death (including euthanasia) have been reported.

To report suspected adverse events, for technical assistance or to obtain a copy of the SDS, contact Zoetis Inc. at 1-888-963-8471

or www.zoetis.com.

For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS

or www.fda.gov/reportanimalae.

CLINICAL PHARMACOLOGY:

Pharmacodynamics:

Vomiting is a complex process coordinated centrally by the emetic center which consists of several brainstem nuclei (area postrema, nucleus

tractus solitarius, dorsal motor nucleus of the vagus) that receive and integrate sensory stimuli from central and peripheral sources and

chemical stimuli from the circulation and the cerebro-spinal fluid. Maropitant is a neurokinin 1(NK

1) receptor antagonist which acts by

inhibiting the binding of substance P, a neuropeptide of the tachykinin family. SubstanceP is found in significant concentrations in the nuclei

comprising the emetic center and is considered the key neurotransmitter involved in emesis.

1By inhibiting the binding of substance P within

the emetic center, maropitant provides broad-spectrum effectiveness against neural (central) and humoral (peripheral) causes of vomiting.

In vivo model studies in dogs have shown that maropitant has antiemetic effectiveness against both central and peripheral emetogens

including apomorphine, and syrup of ipecac.

1Diemunsch P, Grelot L. Potential of substance P antagonists as antiemetics. [Review] [60refs]. Drugs. 2000;60:533-46.

Pharmacokinetics (CERENIA Tablets):

Mean (±SD) Plasma Pharmacokinetic Parameters for Maropitant in Beagle Dogs after single dose and repeat oral doses of

Maropitant:

PK Parameter 2 mg/kg Single

Dose

2 mg/kg repeat

Doses1

8 mg/kg Single

Dose

8 mg/kg

repeat Doses1

Tmax2

(hr)

2.0

(1.5 – 3.0)

1.5

(1.0 – 3.0)

1.5

(1.0 – 3.0)

2.5

(1.5 – 7.0)

Cmax

(ng/mL)

154

(111)

304

(165)

588

(416)

1409

(516)

AUC(0-24)

(ng*hr/mL)

1440

(982)

3890

(3030)

6730

(5030)

26600

(9200)

T1/2 2

(hr)

NC 7.69

(6.21 - 17.8)

NC 25.4

(6.06 - 30.0)

Accumulation Ratio

ac)

NA 2.46

(1.68, 3.61)

NA 4.81

(3.28, 7.05)

1Following once daily doses of maropitant for 14 days.

2Median (Range)

3Ratio=Multiple Dose AUC(

0-24)/Single Dose AUC(0-24 ), Least square means (95% Confidence Interval)

NA= Not Applicable

NC= Not Calculated

Following oral administration, median time to reach Cmax was within 2.5 hr. The absolute bioavailability of maropitant was low (24%) following

oral administration of 2 mg/kg maropitant. After an oral dose, prandial status does not significantly affect the extent of oral bioavailability.

Greater than dose-proportional drug exposure can be expected with an increase in dose (1-16 mg/kg PO). However as doses increase

(20-50 mg/kg PO), the dose proportionality is re-established. Based upon enzyme kinetics, involvement of a high capacity enzyme in vitro

(CYP3A12) may contribute to this return to dose linearity. Due to dose dependent pharmacokinetics, the maropitant concentrations reached

steady state approximately after 4 and 8 days following 2 and 8 mg/kg, respectively. The observed drug accumulation ratios were 2.46

and 4.81, after oral administration of 2 and 8 mg/kg, respectively. The exposure of 10 week old puppies to maropitant was lower than that

observed in adult dogs, particularly after repeat doses of 1 or 2 mg/kg. Systemic clearance of maropitant following IV administration was

970, 995, and 533 mL/hr/kg at doses of 1, 2 and 8 mg/kg, respectively.

Urinary recovery of maropitant and its major metabolite was minimal (<1% each). The hepatic metabolism of maropitant involves two

cytochrome P-450 isoenzymes: CYP2D15 and CYP3A12. In enzyme kinetics data suggest that the non-linear kinetics may be partially in vitro

associated with saturation of the low capacity enzyme (CYP2D15). Plasma protein binding of maropitant was high (99.5%).

Pharmacokinetics (CERENIA Injectable):

CERENIA is formulated using sulphobutylether-ß-cyclodextrin (SBECD), which exhibits enhanced binding to maropitant at refrigerated

temperatures. The enhanced binding afﬁnity reverses rapidly upon warming.

DOGS:

The pharmacokinetic (PK) characterization associated with maropitant after a single oral (PO), intravenous (IV), or subcutaneous (SC) dose

administration in adult Beagle dogs is provided in the table below.

Pharmacokinetic Parameters in Beagle Dogs (Mean±SD or Mean and Range)

PK Parameter SC at 1 mg/kg

(n=8)

IV at 1 mg/kg

(n=8)

PO at 2 mg/kg

(n=8)

PO at 8 mg/kg

(n=8)

AUC0-inf (hr*ng/mL) 759.08±189.49 693.83±137.25 561±322 7840±5600

Cmax (ng/mL) 102.99±46.06 296.62±60.77 81±32 776±604

T1/2

(hr) 8.84 a (6.15-20.48) 6.85 a

(4.87-11.30) 4.03 (2.48-7.09) 5.46 (3.39-7.65)

Tmax (hr) 0.56±0.40 n/a 1.9±0.5 1.7±0.7

a Harmonic mean

The absolute bioavailability of maropitant was much higher following SC injection (91% at 1 mg/kg) than after PO administration (24% at

2 mg/kg). Oral bioavailability may be underestimated due to the presence of nonlinear kinetics and the resulting longer T

1/2 seen after intravenous

(IV) administration. Although hepatic ﬁrst-pass metabolism contributed to the relatively low bioavailability after an oral dose, prandial status does

not signiﬁcantly affect the extent of oral bioavailability. Greater than dose-proportional drug exposure can be expected with an increase in dose

(1–16 mg/kg PO). Systemic clearance of maropitant following IV administration was 1499.13 mL/hr/kg at a dose of 1 mg/kg. An accumulation

ratio of 1.5 was observed following once-daily use of maropitant for ﬁve consecutive days at 1 (SC) or 2 mg/kg (PO). Urinary recovery of maropitant

and its major metabolite was minimal (<1% each). The hepatic metabolism of maropitant involves two cytochrome P-450 isoenzymes: CYP2D15

and CYP3A12. Based on in vitro enzyme kinetics data, it is believed that the non-linear kinetics may be partially associated with saturation of the

low capacity enzyme (CYP2D15). However as doses increase (20–50 mg/kg PO), dose proportionality is re-established.

Based upon enzyme kinetics, involvement of a high capacity enzyme (CYP3A12) may contribute to this return to dose linearity. Plasma in vitro

protein binding of maropitant was high (99.5%).

Based on differences in plasma trough concentrations from a single study, the exposure of 10 week old puppies to maropitant may be lower

than that observed in adult dogs, particularly after doses of 1 or 2 mg/kg.

CATS:

The pharmacokinetic characterization associated with maropitant after a single subcutaneous (SC) or intravenous (IV) dose administration in cats

is provided in the table below.

Pharmacokinetic Parameters for a Single Dose in 6-7 Month Old Cats (Mean±SD or Mean and Range)

PK Parameter SC at 1 mg/kg

(n=6)

IV at 1 mg/kg

(n=6)

AUC0-inf (hr*ng/mL) 2016.07±516.65 2116.53±706.72

Cmax (ng/mL) 257.84±49.95 987.65±421.75

T1/2

(hr) 6.57 a (5.09-8.60) 4.86a (3.44-6.79)

Tmax (hr) 0.43±0.33 n/a

a Harmonic mean

There appears to be an age-related effect on the pharmacokinetics of maropitant in cats; kittens (4 months) have a higher clearance than adults.

In multiple IV and SC studies, the mean maropitant half-life in kittens (4-7 months old) is 7.83 hours, compared to 17.2 hours in adults. The mean

bioavailability of maropitant after subcutaneous administration in cats was 91.3%. The mean total body clearance (CL) and volume of distribution at

steady-state (Vss) determined after IV administration of 1.0 mg/kg to 6 cats was 510 (388 to 603) mL/hr/kg and 2.3 (1.4 to 3.6) L/kg, respectively.

Maropitant displays linear kinetics when administered SC within the 0.25–3 mg/kg dose range. Following SC administration of once daily doses

of 1 mg/kg body weight for 5 consecutive days, accumulation was 250%. Maropitant undergoes cytochrome P450 (CYP) metabolism in the liver.

CYP1A and CYP3A-related enzymes were identiﬁed as the feline isoforms involved in the hepatic biotransformation of maropitant. Renal and fecal

clearances are minor routes of elimination for maropitant, with less than 1% of a 1 mg/kg SC dose appearing in the urine or feces as maropitant.

For the major metabolite, 10.4% of the maropitant dose was recovered in urine and 9.3% in feces. Plasma protein binding of maropitant in cats

was estimated to be 99.1%.

EFFECTIVENESS:

Prevention of Acute Vomiting (CERENIA Tablets)

In laboratory model studies, CERENIA Tablets dosed at a minimum of 2mg/kg BW reduced the number of emetic events associated with

established neural (central) and humoral (peripheral) stimuli. Following administration of apomorphine (central emetic stimuli), vomiting was

observed in 33% (4 of 12) of Beagle dogs treated with CERENIA Tablets and 100% (12of 12) of Beagle dogs treated with placebo tablets.

Following administration of syrup of ipecac (peripheral emetic stimuli) vomiting was observed in 33% (4 of 12) of Beagle dogs treated

with CERENIA Tablets and in 83% (10of 12) of Beagle dogs treated with placebo tablets.

In a study of 275canine patients presented to veterinary hospitals with a history of acute vomiting, dogs were initially administered CERENIA

Injectable Solution or placebo on Day 0. Following the initial dose, dogs allocated to the CERENIA group were treated with either CERENIA

Tablets at a minimum of 2mg/kg orally or Injectable Solution at 1mg/kg subcutaneously once daily at the discretion of the clinician. Dogs

allocated to the placebo group were treated using either an injectable placebo solution or placebo tablets once daily at the discretion of the

clinician. Of the 199dogs included in the analysis for effectiveness, 27of 54dogs (50%) in the placebo group displayed vomiting at some time

during the study and 31of 145dogs (21.4%) in the treated group displayed vomiting during the study period.

Percent Of Vomiting For Each Study Day, Based Upon Treatment And Route Of Administration.

Days Treatment Route # dogs # vomited % vomited

Day 0 Placebo (54) SC 54 15 28%

CERENIA (145) SC 145(143*) 14 10%

Day 1 Placebo (45) PO 22 3 14%

SC 23 16 70%

CERENIA (108) PO 67 2 3%

SC 41 16 39%

Day 2 Placebo (16) PO 7 2 29%

SC 9 6 67%

CERENIA (37) PO 24 0 0%

SC 13 8 62%

Day 3 Placebo (6) PO 2 0 0%

SC 4 1 25%

CERENIA (21) PO 14 0 0%

SC 7 5 71%

Day 4 Placebo (2) PO 1 0 0%

SC 1 1 100%

CERENIA (7) PO 5 0 0%

SC 2 1 50%

Day 5 CERENIA (1) SC 1 0 0%

*2 dogs administered CERENIA were not observed on Day 0. Their vomiting status was unknown. 143was used in the denominator for

% vomited.

In US field studies in veterinary patients, CERENIA Tablets and Injectable Solution were well tolerated in dogs presenting with various

conditions including parvovirus, gastroenteritis, and renal disease. There were no notable differences in mean laboratory values between

CERENIA-treated and placebo-treated patients.

CERENIA Tablets were used safely in dogs receiving other frequently used veterinary products such as fluid and electrolyte replacement

solutions, antimicrobial agents, vaccines, antacids, and antiparasitic agents.

Prevention of Vomiting due to Motion Sickness (CERENIA Tablets)

In a study of canine veterinary patients taken on a one-hour car journey and treated with either CERENIA Tablets at a minimum dose of

8mg/kg BW or placebo tablets 2hours prior to the journey, 67 of 122(55%) of dogs vomited during the journey when treated with placebo

while 8of 122(7%) vomited during the journey after treatment with CERENIA Tablets. The probability that a dog in this study, prone to motion

sickness would NOT vomit during a journey if treated with CERENIA Tablets was 93%, while the probability was 48% if treated with placebo.

CERENIA INJECTABLE:

DOGS:

In laboratory model studies, CERENIA Injectable Solution administered subcutaneously at 1 mg/kg in Beagle dogs reduced the number of emetic

events associated with established neural (central) and humoral (peripheral) stimuli. Following administration of apomorphine (central emetic

stimuli), vomiting was observed in 16.7% (2 of 12) of dogs treated with CERENIA Injectable Solution and 83.3% (10 of 12) of placebo-treated

dogs. Following administration of syrup of ipecac (peripheral emetic stimuli) vomiting was observed in 25% (3 of 12) of dogs treated with

CERENIA Injectable Solution and in 100% (12 of 12) of dogs treated with placebo.

In a study of veterinary cancer patients, dogs were treated with CERENIA Injectable Solution or placebo either 1 hour prior to cisplatin (prevention)

or after the ﬁrst vomiting episode following cisplatin (treatment) and monitored for 5 hours. In the groups evaluated for prevention of vomiting,

94.9% (37/39) of the dogs administered CERENIA Injectable Solution and 4.9% (2/41) of the dogs administered placebo did not vomit. In the

groups evaluated for treatment, 21% (8/38) of the dogs administered CERENIA Injectable Solution and 5.1% (2/39) of the dogs administered

placebo had no further episodes of vomiting following treatment.

Frequency Distribution of Numbers of Vomiting Episodes

For Treatment: Number of Vomiting Episodes Post Injection.

For Prevention: Total Number of Vomiting Episodes.

Number of Vomiting

Episodes

Dogs with Vomiting Episodes* (% of Dogs)

Treatment of Vomiting Prevention of Vomiting

Placebo

(n=39**)

CERENIA

(n=38**)

Placebo

(n=41)

CERENIA

(n=39)

0 2 (5.1) 8 (21.1) 2 (4.9) 37 (94.9)

1 3 (7.7) 7 (18.4) 2 (4.9) 1 (2.6)

2 4 (10.3) 6 (15.8) 3 (7.3) 1 (2.6)

3 3 (7.7) 6 (15.8) 4 (9.8) 0 (0)

4 4 (10.3) 4 (10.5) 3 (7.3) 0 (0)

5 2 (5.1) 5 (13.2) 4 (9.8) 0 (0)

6 14 (35.9) 1 (2.6) 1 (2.4) 0 (0)

7 2 (5.1) 1 (2.6) 12 (29.3) 0 (0)

8 2 (5.1) 0 (0) 5 (12.2) 0 (0)

9 2 (5.1) 0 (0) 2 (4.9) 0 (0)

10 0 (0) 0 (0) 2 (4.9) 0 (0)

11 1 (2.6) 0 (0) 0 (0) 0 (0)

12 NA NA 1 (2.4) 0 (0)

* Dogs that exhibited an unacceptable level of vomiting (6 events) were withdrawn from the study and treated with another antiemetic.

** There were initially 41 and 42 dogs treated with either placebo or CERENIA Injectable Solution, respectively. However, if a dog did not vomit

following cisplatin therapy, it did not receive a post-cisplatin treatment with either placebo or CERENIA Injectable Solution, and hence it was not

considered in the therapeutic evaluation.

In a study of 275 canine patients presented to veterinary hospitals with a history of acute vomiting, dogs were initially administered CERENIA

or placebo on Day 0. Following the initial dose, dogs allocated to the CERENIA group were treated with either CERENIA Tablets at a minimum of

2mg/kg orally or Injectable Solution at 1 mg/kg subcutaneously once daily at the discretion of the clinician. Dogs allocated to the placebo group

were treated using either an injectable placebo solution or placebo tablets once daily at the discretion of the clinician. Of the 199 dogs included

in the analysis for effectiveness, 27 of 54 dogs (50%) in the placebo group displayed vomiting at some time during the study and 31 of 145 dogs

(21.4%) in the CERENIA-treated group displayed vomiting during the study period.

Percent of Vomiting for Each Study Day, Based Upon Treatment and Route of Administration.

Days Treatment Route # dogs # vomited % vomited

Day 0 Placebo (54) SC 54 15 28%

CERENIA (145) SC 145 (143*) 14 10%

Day 1 Placebo (45) PO 22 3 14%

SC 23 16 70%

CERENIA (108) PO 67 2 3%

SC 41 16 39%

Day 2 Placebo (16) PO 7 2 29%

SC 9 6 67%

CERENIA (37) PO 24 0 0%

SC 13 8 62%

Day 3 Placebo (6) PO 2 0 0%

SC 4 1 25%

CERENIA (21) PO 14 0 0%

SC 7 5 71%

Day 4 Placebo (2) PO 1 0 0%

SC 1 1 100%

CERENIA (7) PO 5 0 0%

SC 2 1 50%

Day 5 CERENIA (1) SC 1 0 0%

* 2 dogs administered CERENIA were not observed on Day 0. Their vomiting status was unknown. 143 was used in the denominator for % vomited.

In US ﬁeld studies in veterinary patients, CERENIA Injectable Solution and Tablets were well tolerated in dogs presenting with various clinical

conditions including parvovirus, gastroenteritis, and renal disease. There were no notable differences in mean laboratory values between

CERENIA-treated and placebo-treated patients.

CERENIA Injectable Solution was used safely in dogs receiving other frequently used veterinary products such as fluid and electrolyte

replacement solutions, antimicrobial agents, vaccines, antacids, and antiparasitic agents.

In a laboratory study, thirty-one dogs were subcutaneously administered CERENIA Injectable Solution or saline, at 1 mL/10 kg body weight,

45 minutes prior to administration of an opioid analgesic. Following administration of the opioid analgesic, none of the CERENIA Injectable

Solution treated dogs vomited and 93.8% (15/16) of placebo-treated dogs vomited.

The effectiveness of CERENIA administered at 1 mg/kg IV was demonstrated by bridging the results of a PK study to clinical data supporting

effectiveness of 1 mg/kg administered SC. The IV and SC administration of a single dose of 1 mg/kg maropitant are equivalent, based on the

bioequivalence of the IV and SC AUClast and justiﬁcation for the therapeutic equivalence of the IV and SC C

max.

CATS:

In a ﬁeld study, 195 cats were presented to veterinary hospitals with a history of vomiting associated with various clinical conditions including

gastroenteritis, gastritis, pancreatitis, inﬂammatory bowel disease, neoplasia, and hepatic lipidosis. Cats were treated with CERENIA Injectable

Solution or placebo (in a ratio of 2:1) and observed in the veterinary hospital for 24 hours for the presence of an emetic event(s) deﬁned as the

observation of the act of vomiting or the presence of vomitus. Cats could continue antiemetic treatment every 24 hours for up to 5 consecutive days

at the discretion of the clinician. Of 165 cats included in the analysis for effectiveness, 2 CERENIA Injectable Solution treated cats (1.8%) vomited

1 time each and 10 placebo-treated cats (18.5%) vomited a total of 15 times in the ﬁrst 24 hours post treatment.

Percent of Cats Vomiting for Each Study Day by Treatment

Study Day Treatment # cats # vomited % vomited

Day 0 Placebo 54 10 18.5

CERENIA 111 2 1.8

Day 1 Placebo 20 4 20.0

CERENIA 34 1 2.9

Day 2 Placebo 9 2 22.2

CERENIA 8 0 0.0

Day 3 Placebo 5 0 0.0

CERENIA 5 0 0.0

Day 4 Placebo 3 0 0.0

CERENIA 1 0 0.0

The effectiveness of CERENIA administered at 1 mg/kg IV was demonstrated by bridging the results of a PK study to clinical data supporting

effectiveness of 1 mg/kg administered SC. The IV and SC administration of a single dose of 1 mg/kg maropitant are equivalent, based on the

bioequivalence of the IV and SC AUClast and justiﬁcation for the therapeutic equivalence of the IV and SC C

max.

ANIMAL SAFETY: Laboratory and field studies have demonstrated that CERENIA Tablets are well tolerated in dogs after oral administration.

Target Animal Safety Study for Acute Vomiting (CERENIA Tablets)

Fifty six Beagle dogs (28males and 28females) approximately 16weeks of age were administered CERENIA Tablets orally once daily for

15days at 0, 2, 6, and 10mg/kg. There were 8dogs (4males and 4 females) in the 2 mg/kg group and 16dogs (8males and 8females) in

all other groups. CERENIA Tablets caused decreases in food consumption and body weight that were not dose-dependent and did not persist

after cessation of treatment.

Beagle dogs approximately 8weeks of age were administered CERENIA Tablets orally once daily for 15 days at 0, 2, 6, and 10 mg/kg using

a protocol similar to the previous study. A dose dependent increase in severity of bone marrow hypoplasia was observed histologically.

Interpretation of these study results is complicated by the health status of study animals. Dogs used in the study were weaned early, minimally

acclimated to the test facility, many of the dogs in the study tested positive for coccidia and some tested positive for canine parvovirus.

Beagle dogs approximately 10weeks of age were administered either placebo tablets for 2days, CERENIA Tablets at 8mg/kg for 2days,

placebo (saline) subcutaneously (SC) for 5days, CERENIA Injectable Solution at 1mg/kg SC for 5days, or CERENIA Tablets at 2mg/kg for 5days

(8dogs in each dose group). Mild pain associated with injection was noted in more dogs and lasted longer in dogs that received maropitant

injections compared to saline. Males administered CERENIA at 8mg/kg orally for 2days had a decrease in food consumption. Body weight and

food consumption were variable throughout the 4week acclimation period. Two dogs that received 8mg/kg maropitant orally for 2days were

below the reference range for reticulocyte counts. Decreases in reticulocyte counts were also seen in 4(of 8) placebo treated dogs (SC saline

for 5days). Hypocellular femoral bone marrow described as “minimal” was seen in 1male that received 1mg/kg maropitant SC for 5days;

reticulocyte counts were not available for this dog.

Twenty four Beagle dogs (12 males and 12 females) 7 months of age were administered maropitant at doses of 0, 1, 5, and 20 mg/kg orally

once daily for 93 consecutive days. Maropitant produced sporadic clinical signs (salivation, emesis), body weight loss, and lower serum albumin

levels at 20 mg/kg/day.

Maropitant increased P-R interval, P wave duration, and QRS amplitude in the 20 mg/kg /day dose group.

One female in the 20 mg/kg/day group had increased cellularity of the bone marrow. This female was noted to have lower mean red cell

parameters (red blood cell count, hemoglobin, hematocrit) and higher platelet counts and reticulocytes.

Target Animal Safety Study for Motion Sickness (CERENIA Tablets)

Forty Beagle dogs (20males and 20females) between 16– 18weeks of age were administered CERENIA Tablets orally once daily for 6days

at 0, 8and 24mg/kg. There were 16dogs (8males and 8 females) in the 0and 24mg/kg groups and 8dogs (4males and 4females) in the

8mg/kg group. At 24 mg/kg, CERENIA Tablets caused decreases in food consumption, with decreases in body weight, liver and testis weight;

and an increase in RBC count indicating hemoconcentration, but the effects on feed consumption, body weight, and RBCs did not persist in the

post-treatment recovery period (beyond Day 5).

Beagle dogs approximately 8weeks of age were administered CERENIA Tablets orally once daily for 6days at 0, 8, and 24mg/kg using a

protocol similar to the previous study. One dog in the 24mg/kg/day group died of unknown causes on study day 2and a dose dependent

increase in occurrence and severity of bone marrow hypoplasia and lymphoid depletion was observed histologically. Interpretation of these

study results is complicated by the health status of study animals. Dogs used in the study were weaned early, minimally acclimated to the test

facility, and many of the dogs in the study tested positive for coccidia. Additionally, some dogs in the study tested positive for canine parvovirus,

however, clinical parvoviral disease was not definitively diagnosed.

Tolerance Studies (CERENIA Tablets)

Twenty four Beagle dogs (14males and 10females) between 11and 25weeks of age were administered CERENIA Tablets in 2phases with

8dogs per group. In the first phase the dogs were administered 0, 20or 30 mg/kg orally once daily for 7days and in the second phase 0, 40, or

50mg/kg once daily for 7 days. CERENIA Tablets administered at 20and 30mg/kg caused occasional vomiting. CERENIA Tablets administered

at 40mg/kg and 50mg/kg caused clinically relevant signs of weight loss, vomiting, soft stools, weakness, lethargy, salivation and hypokalemia.

Additionally, leukopenia characterized by a neutropenia and a trend toward decreasing plasma phosphorus values was seen. Decreased heart

rate and prolonged corrected QT intervals were seen in all treatment groups in a dose dependent manner.

Twenty-four Beagle dogs (12 males and 12 females) approximately 28 weeks of age were administered maropitant (mesylate salt) orally once

daily for 90 days at 0, 1, 5, and 20 mg/kg. End of study body weights in the 20 mg/kg group were 8-15% lower than baseline body weights.

DOGS (CERENIA ):Injectable

Laboratory and ﬁeld studies have demonstrated that CERENIA Injectable Solution is well tolerated in dogs after subcutaneous administration.

Fifty six Beagle dogs (28 males and 28 females) approximately 16 weeks of age were administered CERENIA Injectable Solution subcutaneously once

daily for 15 days at 0, 1, 3, and 5 mg/kg. There were 8 dogs (4 males and 4 females) in the 1 mg/kg group and 16 dogs (8 males and 8 females) in all

other groups. The primary treatment-related ﬁndings were injection site reactions. Swelling, thickened skin, or pain at one or more of the injection

sites on one or more days of the study were observed in 6 of 16 animals treated with 3 mg/kg/day and 5 of 16 animals treated with 5 mg/kg/day.

Additionally, the activated partial thromboplastin time (APTT) was prolonged (67.5 seconds, reference range 9-15 seconds) in one male dog in the

1 mg/kg group on study day 15. Relationship of the prolonged APTT to drug administration could not be determined.

Beagle dogs approximately 8 weeks of age were administered CERENIA Injectable Solution subcutaneously once daily for 15 days at 0, 1, 3, and

5 mg/kg using a protocol similar to the previous study. A dose dependent increase in frequency and severity of bone marrow hypoplasia was observed

histologically. One placebo-treated dog died on day 14 of the study and was diagnosed with suppurative pancreatitis and esophagitis. Interpretation

of the study results is complicated by the health status of study animals. Dogs used in the study were weaned early, minimally acclimated to the test

facility, and many of the dogs in the study tested positive for coccidia.

Beagle dogs approximately 10 weeks of age were administered either placebo tablets for 2 days, CERENIA Tablets at 8 mg/kg for 2 days, placebo

(saline) subcutaneously (SC) for 5 days, CERENIA Injectable Solution at 1 mg/kg SC for 5 days, or CERENIA Tablets at 2mg/kg for 5 days (8 dogs

in each dose group). Mild pain associated with injection was noted in more dogs and lasted longer in dogs that received maropitant injections

compared to saline. Males administered CERENIA Tablets at 8 mg/kg orally for 2 days had a decrease in food consumption. Body weight and food

consumption were variable throughout the 4 week acclimatization period. Two dogs that received 8 mg/kg maropitant orally for 2 days were below

the reference range for reticulocyte counts. Decreases in reticulocyte counts were also seen in 4 (of 8) placebo treated dogs (SC saline for 5 days).

Hypocellular femoral bone marrow described as “minimal” was seen in 1 male that received 1 mg/kg maropitant SC for 5 days; reticulocyte counts

were not available for this dog.

Twenty four Beagle dogs approximately 16 weeks of age were administered CERENIA Injectable Solution intravenously once daily for 5 days at 0, 1,

and 3 mg/kg (4 females and 4 males per group). CERENIA Injectable Solution was administered at room temperature over 1-2 minutes. Reaction to

injection was not speciﬁcally recorded. One male dog in the 1 mg/kg group had low hematocrit and white blood cell count on study day 5. One female

dog in the 3 mg/kg group had an increased ﬁbrinogen on study day 5. There were no other clinically relevant ﬁndings during the study, at necropsy

or in histopathology.

CATS (CERENIA Injectable):

Thirty-two domestic short hair cats (16 males and 16 females) approximately 16 weeks of age were administered CERENIA Injectable Solution

subcutaneously once daily for 15 days at 0, 1, 3, and 5mg/kg. There were 8 cats (4 males and 4 females) in each group. Treatment-related, dose

dependent ﬁndings included pain associated with injection of CERENIA Injectable Solution and injection site heat, pain, redness, and ﬁrmness. Pain

on injection was observed in 5% of cats at 0 mg/kg, 50% of cats at 1 mg/kg, and 75% of cats at 3 and 5 mg/kg. Injection site ﬁrmness >10 mm in

diameter was observed at one or more of the injection sites, on one or more days of the study, in 1 of 8 cats at 1mg/kg, 7 of 8 cats at 3 mg/kg, and

7 of 8 cats at 5 mg/kg. There was a statistically signiﬁcant reduction (p=0.0171) in food intake at 5mg/kg compared to cats at 0 mg/kg. One cat

at 5 mg/kg was lethargic on Days 12, 13, and 14 of the study. Increased skin turgor was observed in 1 cat at 3 mg/kg on Days 10 and 11, 1 cat at

3 mg/kg on Day 12, and 1 cat at 5 mg/kg on Day 12. At gross necropsy, there were no treatment-related ﬁndings. Histopathologic evaluation of

injection sites revealed a dose dependent inﬂammatory response.

Twenty-four healthy domestic shorthair cats (12 males and 12 females) approximately 16 weeks of age were administered maropitant at 1 or 3 mg/kg,

or saline at 0.1 mL/kg intravenously once daily for 5 days. CERENIA Injectable Solution was administered at room temperature over 1-2 minutes.

Reaction to injection was not speciﬁcally recorded, but one cat experienced discomfort with accidental extravascular administration. There were

no clinically relevant ﬁndings during the study, at necropsy or in histopathology.

STORAGE CONDITIONS:

CERENIA Tablets should be stored at controlled room temperature 20°–25°C (68°–77°F) with excursions between 15°–30°C (59°–86°F).

CERENIA Injectable Solution should be stored at or below 30°C (86°F), with excursions permitted up to 40°C (104°F). After ﬁrst vial puncture,

CERENIA Injectable Solution should be stored at refrigerated temperature 2-8°C (36-46°F). Use within 90 days of ﬁrst vial puncture. Stopper

may be punctured a maximum of 25 times.

HOW SUPPLIED:

CERENIA peach-colored tablets are scored with a break line, and contain 16, 24, 60 or 160 mg of maropitant as maropitant citrate per tablet.

Each tablet is marked with “MPT” and the tablet strength.

Each tablet size is available in the following strengths and are supplied in blister packs containing 4 tablets:

16 mg contains 10 blisters per carton (40 tablets)

24 mg contains 10 blisters per carton (40 tablets)

60 mg contains 10 blisters per carton (40 tablets)

160 mg contains 5 blisters per carton (20 tablets)

CERENIA Injectable Solution is supplied in 20 mL amber glass vials. Each mL contains 10 mg of maropitant as maropitant citrate.

Approved by FDA under NADA # 141-262

Approved by FDA under NADA # 141-263

Distributed by:

Zoetis Inc.

Kalamazoo MI 49007

Based on Cerenia Tablets PI

8840540, Revised January 2022; and

Cerenia Injectable Solution PI

40025587, Revised April 2020

8840540

/40025587A&P

Product specificaties

Merk:	Zoetis
Categorie:	Niet gecategoriseerd
Model:	Cerenia

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