Difference between revisions of "Lizard Formulary - Disclaimer"

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==Introduction==
 
 
The following drug dosages are taken from multiple sources and neither their efficacy nor safety can be assured since the information may have been extrapolated from animals other than lizards. There will be interspecific variation.
 
The following drug dosages are taken from multiple sources and neither their efficacy nor safety can be assured since the information may have been extrapolated from animals other than lizards. There will be interspecific variation.
  
*Since lizards are poikilothermic, their metabolism is affected by the ambient temperature. The pharmacokinetics of any drug will therefore vary with the temperature. The lizard will need to be kept at the higher end of its POTZ.
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Since lizards are poikilothermic, their metabolism is affected by the ambient temperature. The pharmacokinetics of any drug will therefore vary with the temperature. The lizard will need to be kept at the higher end of its [[Preferred optimum temperature zone|preferred optimum temperature zone (POTZ)]].
*There are no drugs preparations licensed for reptiles. Drugs licensed for use in other species may be administered under the responsibility of the veterinary surgeon who has the lizard 'under his care'.
+
There are no drugs preparations licensed for reptiles. Drugs licensed for use in other species may be administered under the responsibility of the veterinary surgeon who has the lizard 'under his care'.
  
==Antimicrobials==
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*[[Lizard Formulary - Antimicrobials|Antimicrobials]]
 
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*[[Lizard Formulary - Antifungals|Antifungals]]
Sample all suspected infections for microscopy, culture and sensitivity. The majority of bacterial infections in lizards are by Gram-negative organisms, particularly Enterobacteriacae. Therapy may be required before the results of bacterial sensitivity tests are known.
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*[[Lizard Formulary - Antiparasitic|Antiparasitic]]
 
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*[[Lizard Formulary - Anaesthesia Associated Drugs|Anaesthesia associated drugs]]
*Aminoglycosides and quinolones are effective against most aerobic pathogens and there is little bacterial resistance to them.
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*[[Lizard Formulary - Hormones|Hormones]]
*The fluoroquinolone derivative enrofloxacin is bacteriocidal (inhibit microbial DNA gyrase) and is well distributed to tissues. It is active against a wide range of Gram-negative organisms as well Gram-positives and Mycoplama spp. It is not effective against anaerobes.
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*[[Lizard Formulary - Nutritional Support|Nutritional support]]
*Carbenicillin and ceftazidime are good broad-spectrum antibiotics useful against anaerobes as well as most Gram-negative pathogens. If Pseudomonas spp. and anaerobes are present, ceftazidime is the most appropriate choice.
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*[[Lizard Formulary - Miscellaneous Agents|Miscellaneous agents]]
 
+
[[Category:Lizard_Formulary|A]]
The following has also been advised: amikacin in combination with ampicillin for respiratory infections; chloramphenicol for gastrointestinal infections; an aminoglycoside in combination with a broad spectrum penicillin for general systemic infections.
 
*All aminoglycosides may affect neuromuscular transmission leading to muscle weakness and cause nephrotoxicity especially in reptiles kept at more than 25°C. They are also more toxic in gravid females.
 
 
 
Any antibiotic therapy, but particularly gentamycin, should be accompanied by fluids to maintain adequate renal function and reduce the possibility of nephrotoxicity.
 
 
 
===Amikacin===
 
*Potentially nephrotoxic but no published data
 
*Administer fluids concurrently
 
*Frequently used with a penicillin or a cephalosporin
 
*2.5 mg/kg IM then 2.5-5 mg q72h
 
*50 mg/10ml saline x 30 min nebulisation q12h
 
*Maintenance temperature if species POTZ unknown is 25°C
 
 
 
===Amoxicillin===
 
*Use with an aminoglycoside
 
*20 mg/kg SC, IM q24h
 
*Maintenance temperature if species POTZ unknown is 26°C
 
 
 
===Ampicillin===
 
*May be used with an aminoglycoside
 
*3-6 mg/kg PO q12-24h
 
*3-10 mg/kg IM, SC q12-24h
 
 
 
===Carbenicillin===
 
*May be used with an aminoglycoside but at different time of day
 
*400 mg/kg IM, SC q24h
 
*Maintenance temperature if species POTZ unknown is 30°C
 
 
 
===Cefoperazone===
 
*Published data in tegus
 
*125 mg/kg IM q24h
 
 
 
===Cefotaxime===
 
*May be used with an aminoglycoside
 
*20-40 mg/kg IM q24h
 
*100 mg/10ml saline x 30 min nebulisation q12h
 
 
 
===Ceftazidime===
 
*20 mg/kg IM q72h
 
*Maintenance temperature if species POTZ unknown is 30°C
 
 
 
===Cefuroxime===
 
*50 mg/kg IM q48h
 
*Maintenance temperature if species POTZ unknown is 30°C
 
 
 
===Cephuroxime===
 
*50 mg/kg IM q48h
 
 
 
===Cephalexin===
 
*20-40 mg/kg PO q12h
 
 
 
===Cephaloridine===
 
*10 mg/kg IM, SC q12h
 
 
 
===Cephalothin===
 
*20-40 mg/kg IM q12h
 
 
 
===Chloramphenicol===
 
*May cause pigmentation changes in chameleons
 
*20 mg/kg PO, IM, SC q12h
 
*40mg/kg PO, IM, SC q24h
 
 
 
===Chlortetracycline===
 
*200mg/kg PO 24h
 
 
 
===Ciprofloxacin===
 
*11 mg/kg PO q48-72h
 
 
 
===Clindamycin===
 
*2.5-5 mg/kg PO q12h
 
*5 mg/kg PO q24h
 
 
 
===Dihydrostreptomycin===
 
*Administer fluids concurrently
 
*5 mg/kg IM q12-24h
 
 
 
===Dimetridazole===
 
*40 mg/kg PO q24h 5d
 
 
 
===Doxycycline===
 
*5-10 mg/kg PO q24h 10-45d
 
 
 
===Enrofloxacin===
 
*5-10mg/kg q24h PO, IM, SC, ICo
 
*1-3 ml of 50 mg/250ml sterile water for nasal flush q12-24h with parenteral antibiotics
 
 
 
===Gentamycin===
 
*Do not use in animals over 20kg
 
*2.5 mg/kg SC q72h
 
*10-200 mg/15ml saline x 30 min nebulisation q12h
 
*Maintenance temperature if species POTZ unknown is 24°C
 
 
 
===Kanamycin===
 
*Administer fluids concurrently
 
*10 mg/kg SC, IM, IV q24h
 
*Maintenance temperature if species POTZ unknown is 24°C
 
 
 
===Lincomycin===
 
*Potentially nephrotoxic
 
*Administer fluids concurrently
 
*6 mg/kg q12-24h
 
 
 
===Metronidazole===
 
*May be administered concurrently with amikacin
 
*Low dose may stimulate depressed immune system
 
*12.5-40 mg/kg q24h > 7d
 
*100-275 mg/kg PO as a single dose
 
 
 
===Oxytetracycline===
 
*May produce local reaction at injection site
 
*6-10 mg/kg IM, IV q24h
 
 
 
===Penicillin, benzathine , benzathine===
 
*May be administered concurrently with amikacin
 
*10,000 units/kg IM q48-96h
 
 
 
===Penicillin G===
 
*Infrequently used
 
*10,000-20,000 units/kg IM, SC, IV, ICo q8-12h
 
 
 
===Piperacillin===
 
*Administer fluids concurrently
 
*May be used with an aminoglycoside
 
*50-100 mg/kg IM q24h
 
*100-200 mg/kg IM q24-48h in chameleons
 
*100 mg/10ml saline x 30 min nebulisation q12h
 
 
 
===Streptomycin===
 
*Potentially nephrotoxic
 
*Administer fluids concurrently
 
*Avoid with renal/hepatic dysfunction
 
*10 mg/kg IM q12-24h
 
 
 
===Sulphadiazine===
 
*Administer fluids concurrently
 
*Do not use with renal impaired animals
 
*25 mg/kg PO q24h
 
 
 
===Sulphadimethoxine===
 
*Potentially nephrotoxic
 
*Administer fluids concurrently
 
*90 mg/kg IM then 45 mg/kg q24h
 
 
 
===Tetracycline===
 
*May disturb the normal intestinal microflora
 
*10 mg/kg PO q24h
 
 
 
===Ticarcillin===
 
*Administer fluids concurrently
 
*50-100 mg/kg IM q24h
 
 
 
===Tobramycin===
 
*Potentially nephrotoxic
 
*Administer fluids concurrently
 
*Potentiated by â-lactams
 
*2 mg/kg IM q24h
 
*2.5 mg/kg IM q12h in chameleons
 
 
 
===Trimethoprim/sulphadiazine===
 
*Administer fluids concurrently
 
*15 mg/kg IM q24
 
 
 
===Trimethoprim/sulphamethoxaline===
 
*Administer fluids concurrently
 
*10-30 mg/kg PO q24h
 
 
 
===Tylosin===
 
*Reported useful for mycoplasma respiratory infections
 
*5 mg/kg IM q24 10-60d
 
 
 
==Antifungals==
 
Fungal infections are not uncommon in reptiles and can be the primary disease agent or secondary in already compromised individuals. Antifungal drugs may be useful but treatment regimens have not been established adequately.
 
 
 
Amphotericin- B
 
Potentially nephrotoxic
 
Can be used with ketaconazole
 
Administer slowly
 
0.5 mg/kg IV q48-72h
 
5 mg/150ml saline x 1h nebulisation q12h 7d
 
 
 
Fluconazole
 
5 mg/kg PO q24h
 
 
 
Griseofulvin
 
Limited success
 
20-40 mg/kg PO q72h 5 Rxs
 
 
 
Itraconazole
 
Has been used in spiny lizards (Sceloporus spp.) at 23.5 mg/kg
 
 
 
Ketaconazole
 
Potentially hepatotoxic
 
15-30 mg/kg PO q24h 2-4w
 
 
 
Nystatin
 
100,000 IU/kg PO q24h 2-4 w
 
 
 
==Antiparasitic==
 
Parasitic infections are common in lizards especially wild caught specimens.
 
 
 
Environmental treatment is important.
 
 
 
Albendazole
 
Antinematode
 
50 mg/kg PO as a single dose
 
 
 
Emetine
 
Antiamoeba, antitrematode
 
0.5 mg/kg IM, SC q24h 10d
 
 
 
Fenbendazole
 
Antinematode
 
100 mg/kg PO as a single dose
 
 
 
Ivermectin
 
Antinematode, antiascarid
 
May cause skin discoloration at injection site in chameleons
 
Not for use in chelonia
 
-0.2 mg/kg IM, SC, PO
 
Repeat as appropriate
 
 
 
Levamisole
 
Antinematode including lungworms
 
Avoid concurrent use with chloramphenicol
 
Avoid in debilitated animals
 
Low dose may stimulate depressed immune system
 
Can be used IM but less effective
 
10 mg/kg SC, ICo, repeat in 2 weeks
 
200 mg/kg PO as a single dose
 
 
 
Metronidazole
 
antiprotozoal
 
100 mg/kg PO q3d 2-3w
 
125-250 mg/kg PO, repeat in 2 weeks
 
40 mg/kg PO, repeat in 2 weeks for trichomonad ocular lesions in geckos
 
200 mg/kg PO, repeat in 2 weeks for trichomonad SC lesions in geckos
 
 
 
Nitrofurazone
 
Anticoccidia
 
Seldom used
 
25.5 mg/kg PO
 
 
 
Oxfendazole
 
Antinematode
 
68 mg/kg PO as a single dose
 
 
 
Paronomycin
 
Antiamoeba
 
35-100 mg/kg PO q24h up to 4w
 
 
 
Praziquantel
 
Anticestode, antitrematode
 
3.5-7.5 mg/kg SC
 
100 mg/kg PO
 
 
 
Pyrantel palmoate
 
Antinematode
 
5mg/kg PO, repeat in 2w
 
 
 
Sulphadiazine, sulphamerazine
 
Anticoccidia
 
Administer fluids concurrently
 
Do not use with renal impaired animals
 
25 mg/kg PO q24h 3w
 
50 mg/kg q24h 3d, then 3d off, then 3d on
 
75 mg/kg PO then 45 mg/kg q24h 5d
 
 
 
Thiabendazole
 
Antinematode
 
50-100 mg/kg PO, repeat in 2w
 
 
 
==Anaesthesia associated drugs==
 
Acetylpromazine
 
Pre-anaesthetic
 
0.05-0.5 mg/kg
 
 
 
Alphadolone/alphaxalone
 
Saffan 3 mg/ml alphadolone and 9 mg/ml alphaxalone giving a 12mg/ml solution
 
Induction and maintenance of general anaesthesia
 
6-9 mg/kg IV
 
9-15 mg/kg IM
 
Incremental doses according to the animal's response
 
 
 
Atropine
 
Pre-anaesthetic
 
Use with bradycardia
 
0.01-0.1 mg/kg IM,SC
 
 
 
Buprenorphine
 
Analgesic
 
0.005-0.02 mg/kg IM q24-48h
 
 
 
Butorphanol
 
Analgesic
 
No established dose
 
 
 
Diazepam
 
No established dose
 
 
 
Doxapram
 
Respiratory stimulant
 
5 mg/kg IV
 
 
 
Halothane
 
Gaseous anaesthetic
 
3-4% induction
 
1.5-3% maintenance
 
 
 
Isoflurane
 
Inhalational anaesthetic of choice
 
Less hepatotoxic than other inhalants
 
Rapid induction and recovery in lizards
 
Up to 6% induction
 
2-3% maintenance
 
 
 
Ketamine
 
Muscle relaxation and analgesia may be marginal
 
Prolonged recovery with higher doses
 
Larger reptiles require lower dose
 
Painful at injection site
 
Questionable safety in debilitated animals
 
Avoid use with renal impairment
 
Lizards require lower dose than other reptiles
 
10-30 mg/kg IM as a sedative, facilitates intubation
 
Useful in large lizards (11.6 mg/kg) in combination with midazolam (0.34-0.35 mg/kg)
 
 
 
Lignocaine
 
Local anaesthetic
 
 
 
Midazolam
 
May be useful in some species
 
2 mg/kg
 
 
 
Pentobarbitone
 
Euthanasia
 
60 mg/kg IV, ICo
 
 
 
Propofol
 
Injectable anaesthetic of choice
 
Rapid induction and rapid recovery
 
10 mg/kg IV
 
Additional doses of 10% of the original may be administered for maintenance
 
 
 
Tiletamine/ zolazepam
 
Not generally used but useful in larger lizards
 
5.5 mg/kg in a 55kg komodo dragon (Varanus komodoensis) led to easy handling within 30 minutes but heavy sedation the day after the anaesthetic
 
10-40 mg/kg IM- 8-20 minute induction, 2-10 hour recovery in smaller individuals
 
 
 
Xylazine
 
Infrequently used
 
0.1-1.25 mg/kg IV, IM
 
 
 
==Hormones==
 
Arginine vasotocin
 
Use in dystocia
 
Administer after calcium
 
More effective than oxytocin
 
0.01-1.0 mg/kg IV, ICo
 
 
 
Calcitonin
 
May be useful in MBD
 
Administer after calcium supplementation
 
Do not use if hypocalcaemic
 
Administer fluids concurrently
 
50 IU IM and repeat in 2w
 
 
 
Dexamethasone
 
Septic/traumatic shock
 
0.6-1.25 mg/kg IV,IM
 
 
 
Oxytocin
 
Dystocias
 
Administer after calcium supplementation
 
2-5 Iu/kg IM
 
 
 
Prednisolone
 
Septic/traumatic shock
 
5-10mg/kg IV, IM
 
 
 
==Nutritional support==
 
Calcium borogluconate
 
MBD
 
Hypocalcaemia
 
Hypocalcaemic dystocia
 
10-50 mg/kg IM, SC, ICo
 
 
 
Calcium carbonate
 
PO
 
 
 
Calcium glubionte
 
MBD
 
Hypocalcaemia
 
Hypocalcaemic dystocia
 
10-50 mg/kg PO
 
 
 
Calcium gluconate
 
MBD
 
Hypocalcaemia
 
Hypocalcaemic dystocia
 
100-200 mg/kg IM, SC, ICo
 
 
 
Calcium lactate / calcium glycerophosphate
 
MBD
 
Hypocalcaemia
 
Hypocalcaemic dystocia
 
1-25 mg/kg IM, SC
 
 
 
Vitamin A
 
Hypovitaminosis A
 
Overdose will cause epidermal sloughing
 
1,000-2,000 IU/kg IM, SC q7d 2-6w
 
 
 
Vitamin B complex
 
Hypovitaminosis B
 
Appetite stimulant
 
5-10mg/kg IM,SC
 
 
 
Vitamin B12
 
Appetite stimulant
 
0.05 mg/kg IM,SC
 
 
 
Vitamin C
 
Supportive treatment for bacterial infections
 
Ulcerative stomatitis
 
10-20 mg/kg IM,Sc q24h
 
100-250 mg/kg PO q24h
 
 
 
Vitamin D3
 
MBD
 
Hypocalcaemia
 
Herbivores sensitive to excess
 
Give PO preferably
 
100 IU/kg IM, repeat in 1w
 
200 IU/kg IM, repeat in 4w
 
200 IU/kg PO q7d
 
 
 
Vitamin E
 
Hypovitaminosis E
 
50-100 mg IM
 
 
 
Vitamin K1
 
Hypovitaminosis K
 
May aid formation of clotting factors
 
0.25-0.50 mg/kg IM
 
 
 
==Miscellaneous agents==
 
 
 
===Allopurinol===
 
*Decreases production of uric acid
 
*Dose not established
 
 
 
===Aminophylline===
 
*Bronchodilator
 
*2-4 mg/kg IM
 
 
 
===Atropine===
 
*OP toxicity
 
*0.1-0.2 mg/kg IM
 
 
 
===Cimetidine===
 
*Gastric and duodenal ulcerations
 
*Oesophageal and gastric reflux
 
*4 mg/kg PO, IM q8-12h
 
 
 
===Flunixin meglumine===
 
*Non-steroidal anti-inflammatory
 
*0.1-0.5 mg/kg IM, SC q12-24h 1-2d
 
 
 
===Furosemide===
 
*Diuretic
 
*5 mg/kg PO, IM, IV q12-24h
 

Latest revision as of 22:08, 26 October 2010


The following drug dosages are taken from multiple sources and neither their efficacy nor safety can be assured since the information may have been extrapolated from animals other than lizards. There will be interspecific variation.

Since lizards are poikilothermic, their metabolism is affected by the ambient temperature. The pharmacokinetics of any drug will therefore vary with the temperature. The lizard will need to be kept at the higher end of its preferred optimum temperature zone (POTZ). There are no drugs preparations licensed for reptiles. Drugs licensed for use in other species may be administered under the responsibility of the veterinary surgeon who has the lizard 'under his care'.