Antidotes
Antidotes
Antidotes
Definition:
A therapeutic substance used to counteract
the toxic action(s) of a specified xenobiotic
WHO/IPCS Classification of
antidotes
Category A : Required to be immediately
available (within 30 minutes)
Examples are; Cyanide antidotes
Methylene blue
Naloxone
Ethanol
Category B: (Required to be
available within 2 hours)
Examples: Deferoxamine
N-acetyl cysteine
Flumazenil
Pralidoxime (2-PAM)
Indications
Acute allergic reactions,
bronchoconstriction, laryngeal
edema
Convulsions, excitation,
anxiety, hypertonia
Anaphylactic shock, cardiac
arrest
Fluid retention, LVF
Indications
Hypoglycemia
Hypoxia
Cardiac arrhythmias
Cerebral oedema, Fluid
retention
Hypotension
Activated Charcoal
It is a fine black odorless powder
Produced in a two-step process
First step is pyrolysis of carbonaceous
materials such as wood, coconut etc.
Followed by treatment at high temperatures
with a variety of activating (oxidizing agents)
such as steam or carbon dioxide to increase its
adsorptive capacity by forming an internal
maze of pores with a huge surface area
Activated Charcoal
It decreases the systemic absorption of a number of
drugs like aspirin, acetaminophen, barbiturates,
phenytoin, cyclic antidepressants and organic
materials
It is administered as a slurry in water, more
palatable preparations are available
Activated Charcoal
Single Dose: 1gm/kg orally or by gastric tube
Repeat dose: 15-20 gm every 4-6 hours if the
amount of the drug ingested is greater than
one-tenth of the usual charcoal dose e.g. an
aspirin ingestion of more than 6-10 gm.
Contraindications:
GI ileus or obstruction
Acid or alkali ingestion
Activated Charcoal
Adverse effects:
- Constipation ( can be prevented by coadministration of a cathartic)
- Distension of stomach with potential risk of
aspiration
- Intestinal bezoars with obstruction
Atropine
Mechanism of action: It is a parasympatholytic agent
which blocks the action of acetylcholine at
muscarinic receptors
Indications:
1. Correction of bronchorrhea and excessive
salivation in OP and Carbamate poisoning
2. To improve heart rate in drug induced atrioventricular conduction impairment e.g. digitalis,
beta blockers, OP and carbamate poisoning
Atropine
Adverse Effects:
- Dryness of mouth, blurred vision, cycloplegia,
mydriasis, urinary retention, tachycardia,
aggravation of angina, constipation
Dose:
OP and Carbamate poisoning: 1-5 mg stat. Repeat
every 5-10 minutes till atropinization is
achieved
- Heart rate more than 100/minute, clear lungs,
normal bowel sounds and pupils at mid point
Atropine
Dose for Drug induced bradycardia:
For adults 0.5-1mg I/V. Repeat as needed. 3 mg is
full vagolytic dose for adults
Formulations:
Atropine sulfate injection 0.6mg/ml
Infusion of 100 ml bottles containing 1mg/ml
Acetyl Cysteine
(N-acetyl cysteine, NAC)
Mechanism of action: It is a sulfhydryl group
donor substituting for the livers usual
sulfhydryl donor Glutathione
Indications:
Acetaminophen (paracetamol) overdose
Other hepatotoxic agents like Carbon
tetrachloride, Ethylene dibromide
Acetyl Cysteine
(N-acetyl cysteine, NAC)
Dosage : Oral
Loading dose :140 mg/kg of the 10% or 20%
solution diluted to 5% in juice or soda
Maintenance dose: 70 mg/kg every 4 hours for 17
doses or 6 doses if no evidence of hepatotoxicity
Intravenous administration: Dosage regime is
given alongwith the drug.
In UK, it is 150 mg/kg in 500 ml of D5W over 4
hours, then 100 mg/kg in 1000 ml of D5W over
16 hours
Flumazenil
Mechanism of action: Highly selective antagonist of
benzodiazepine receptors
Indications:
1. Rapid reversal of benzodiazepine overdose
induced coma and respiratory depression, both
as a diagnostic tool and potential substitute of
endo-tracheal intubation.
2. Post operative reversal of benzodiazepine
sedation for surgical procedures and as an
adjunct in weaning patients from ventilators
Flumazenil
Adverse Effects:
1. Acute withdrawal in benzodiazepine addicts
(hyperexcitability, tacchycardia)
2. May precipitate seizures or arrhythmias in patients
with cyclic antidepressants overdose
Dosage:
1. Benzodiazepine overdose: Administer 0.2 mg I/V,
repeat every 30 seconds to a maximum of 3 mg.
2. Reversal of anaesthetic dose of benzodiazepine:
0.2 mg given intravenously is usually enough
Naloxone
Mechanism of action: It is a pure opioid antagonist
with no agonist activity
Indications:
1. Reversal of acute opioid intoxication manifested
by coma, respiratory depression or hypotension
2. Empiric therapy for stupor or coma suspected to
be caused by opioid overdose
Dose: 0.4-2 mg I/V, may repeat at 2-3 minute
intervals. Maximum dose is 10-15 mg
Naloxone
Adverse effects: Relatively Safe drug
1. In opioid addict may precipitate withdrawal
syndrome.
2. Do not give if the patient is agitated. Give only
if there is altered sensorium with resp. rate less
than 12 and pupillary constriction
Methylene blue
Blue dye used in acute methemoglobinemia
Converts methemoglobin to hemoglobin
Available in 10ml ampules containing
10mg/ml
Dose : 1-2mg/kg slowly I/V over 5 minutes
Maximum dose : 7 mg/kg
Chelating Agents
Certain organic compounds are capable of forming
coordinate bonds with metals through two or more
atoms of the organic compound; such organic
compounds are called chelating agents. The
compound formed by a chelating agent and a
metal is called a chelate. A chelating agent that has
two coordinating atoms is called bidentate; one
that has three, tridentate;
Chelating Agents
Calcium disodium EDTA: Given by parenteral
route ,used in lead poisoning
May cause nephrotoxicity and Zinc depletion
Penicillamine: available by oral route, effective
in chelating lead, mercury and copper, may cause
allergic reactions, weekly measurement of metals
is needed to know the need for continued
therapy, treatment may be given for 3 months
Chelating Agents
BAL (Dimercaprol, British antilewisite)
Used for arsenic, mercury and lead and gold
poisoning, has to be given by deep I/M injection
causes many adverse effects
DMSA (Succimer,2,3-dimercaptosuccinic acid)
It is a water soluble analog of Dimercaprol. Used
in lead and mercury poisoning. Also used in
arsenic poisoning. Available both as oral and
parenteral preparations. Less toxic as compared
to BAL