Agad Tantra Notes
Agad Tantra Notes
व्यवहार आयुवेद
एवुुं ववविवैद्यक
PART A
CHAPTER I: Agada-Tantra & Visha
Agada-Tantra
Nirukti:
- Agada + Tantra = Agada-Tantra
- Agada is the antidote of Gada (poison).
- Tantra is a science.
Scope of Agada-Tantra:
- Protection of healthy individuals from poisons.
- Management of individuals afflicted with poisons.
Prayayavachi:
- Agada = Bheshajam, Bhaishajyam, Aushadham, Jayuh
- Agada-Tantra = Damstra vijnana, Visha-tantra, Visha-gara-vairodhika prashamana,
Jangali
Astanga Ayurveda:
Agada-Tantra is one of the 8 branches of Ayurveda.
Shalya-Tantra Surgery
Paribhasha:
- Visha is the poison which induces toxic symptoms in the body when consumed in
unpurified form or improper quantity.
- Sthavara Visha is the poison present in tubers, roots, etc. such as Kalakuta,
Indravatsa, Shringi and Halahala.
Jangama Visha is the poison present in snakes, spiders, etc.
(अ-हृ - उ - ३५ / ४-५)
B) Based on Sthana:
a) Sthanika (Local)
b) Sarvadaihika (General)
Visha Vega:
Visha crossing over each of the seven Kalas (limitating membranes) successively,
situated in the midway region between two Dhatus, produces different phases of
effect. This is termed as Visha Vega (velocity of poison).
The interval which appears while poison is driven by Vayu from one Kala to another is
known as Vega-antara (interval between phases).
Number of Vegas:
Acharya Charaka Acharya Sushruta
Human Beings 8 7
Animals 4 4
Birds 3 3
Acharya Sushruta has mentioned only 7 Vegas for Humans. There are seven Kalas in
the body, and these Vegas (stages) appear when the Visha crosses the Kalas
successively. After Saptama Vega, the Visha which spread by bite, returns back to
Damshadesha (site of bite), and the Visha consumed orally returns to the Hridaya
(heart) to cause death of the patient as the final stage.
Thus, there is no contradiction between number of Vega of Acharya Charaka &
Acharya Sushruta.
Visha Vega Lakshana - Humans Chikitsa
Prathama Trishna, Moha, Dantaharsha (tingling Dahana karma; Rakta sravana;
Vega sensation in the teeth), Praseka Vamana karma;
(salivation), Chardi, Klama Shitambu sechana; Agada yoga with
Madhu & Ghrita
Tritiya Mandala (circular eruptions), Kandu, Ksharagada with Madhu & Ambu;
Vega Shvayathu (oedema), Kotha (urticaria) Agada Dravya; Nasya; Anjana
Shanka-Visha: (च - वच - २३ / २२१-२२३)
When a person is bitten by something (non-poisonous) in the pitch darkness, the fear
or suspicion (Shanka) of being bitten by a poisonous creature causes manifestation of
symptoms such as Jvara, Chardi, Murccha, Daha, Glani, Moha & Atisara.
This condition is called Shanka-Visha.
For the treatment of this ailment, the wise physician should console the patient.
He should be given Sharkara, Shuddha Gandhaka, Draksha, Payasya, Madhuka and
Madhu along with Mantraputa Ambu (incanted water). The water should also be
sprinkled over the patient’s body. He should be consoled and made cheerful.
Toxicology
Definition:
Toxicology is the science of poisons which deals with their source, toxicity & lethal
dose, chemical composition, action, treatment and antidotes.
Branches of Toxicology:
- Forensic Toxicology
- Pharmacological Toxicology
- Clinical Toxicology
- Regulatory Toxicology
Poisons
Definition:
A poison is a substance which, on ingestion, inhalation, absorption, application or
injection produces injury to the body by its chemical action.
Poisons used for homicidal purpose are aconite, arsenic, oleander, madar, etc.
Opium is sometimes used to kill children.
A homicidal poison is easily accessible, might be colourless, odourless, tasteless and
is therefore easy to administer in drinks and food items.
Homicidal poisons are quick in action and difficult to diagnose.
Classification of Poisons:
A) Medico-legal Classification
i) Suicidal
ii) Homicidal
iii) Cattle
iv) Drug dependence
v) Accidental
vi) Abortifacients
vii) Stupefying
viii) Food poisoning
B) Symptomatic Classification
i) Corrosives - Mineral acids, Organic acids, Vegetable acids
ii) Irritants - Inorganic (metallic & non-metallic)
- Organic (vegetable & animal)
- Mechanical
iii) Neurotics - Cerebral, Spinal, Peripheral
iv) Cardiac poisons
v) Asphyxia
vi) Miscellaneous - Analgesics, Antipyretics, Antihistamines, Tranquilizers,
Antidepressants, Stimulants, Street & Designer drugs
i) Corrosives
Corrosive poisons are highly active irritants which produce both inflammation
and ulceration of tissues. This group consists of strong acids and alkalis.
ii) Irritants
Irritant poisons produce symptoms of pain in the abdomen, vomiting and
purging.
iii) Neurotics
Neurotic poisons act on CNS & PNS. Symptoms usually consist of headache,
drowsiness, giddiness, delirium, stupor, coma, and convulsion.
v) Asphyxia
Asphyxial poisons are inert gases or vapors that displace oxygen from air
when present in high concentrations. They mainly act on the Respiratory
System and may cause symptoms such as dizziness, dyspnoea, headache,
nausea, vomiting, tachycardia and stupor.
Action of poisons:
i) Local action = Poisons act directly on the tissues and cause corrosion, irritation and
inflammation (e.g.: Bhallataka)
ii) Remote action = Poison gets absorbed systematically and acts on CNS, heart, etc.
(e.g.: Snake bite / Scorpion sting)
iii) Combined action = Local & Remote
Route of administration:
i) Enteral - Oral, Anal
ii) Parenteral - Intradermal, Intravenous, Intraosseous, Intra-arterial, Intramuscular,
Subcutaneous, Inhalation
a) Absorption
Absorption may occur through the alimentary tract, skin, lungs, via the eye,
mammary gland, or uterus, as well as from sites of injection. Toxic effects may be
local, but the toxicant must be dissolved and absorbed to some extent to affect the
cell. Solubility is the primary factor affecting absorption. Insoluble salts and ionized
compounds are poorly absorbed, whereas lipid-soluble substances are generally
readily absorbed, even through skin.
b) Distribution
Distribution or translocation of a toxicant is via the bloodstream to reactive sites,
including storage depots. The liver receives the portal circulation and is the organ
most commonly involved with intoxication (and detoxification). The selective deposit
of foreign chemicals in various tissues depends on receptor sites. Ease of chemical
distribution depends largely on its water solubility. Polar or aqueous-soluble agents
tend to be excreted by the kidneys; lipid-soluble chemicals are more likely to be
excreted via the bile and accumulate in fat depots. The highest concentration of a
toxin within an animal is not necessarily found in the organ or tissue on which it
exerts its maximal effect (the target organ). Lead may be found in highest
concentrations in bone, which is neither a site for toxic effects nor a reliable tissue
for toxicological interpretation. Knowledge of the translocation characteristics of
toxicants is necessary for proper selection of organs for analysis.
c) Metabolism
Metabolism or biotransformation of toxicants by the body is an “attempt to
detoxify.”
There are two phases of metabolism. Phase I includes oxidation, reduction, and
hydrolysis mechanisms. These reactions, catalyzed by hepatic enzymes, generally
convert foreign compounds to derivatives for Phase II reactions.
Phase II principally involves conjugation or synthesis reactions. Usually, a fraction is
excreted unchanged, and the rest is excreted or stored as metabolites. Increased
tolerance to subsequent exposures of a toxicant, in some instances, is due to enzyme
induction initiated by the previous exposure.
d) Excretion
Excretion of most toxicants and their metabolites is by way of the kidneys. Some
excretion occurs in the digestive tract and some via milk.
Toxicants are removed in the kidney by glomerular filtration, tubular excretion by
passive diffusion, and active tubular secretion.
The damage to the kidney from the excretion of xenobiotic is specific to the anatomic
location where the excretion occurs. Excretion sites are proximal tubules, glomeruli,
medulla, papilla, and loop of Henle. The proximal convoluted tubule is the most
common site of toxicant-induced injury.
The elimination or disappearance (by metabolic change) of a chemical from an organ
or the body is expressed in terms of half-life (t½), defined as the amount of time
required for the disappearance of half of the compound. The rate of elimination
usually depends on the concentration of the compound, and different body
compartments will likely have different elimination rates.
Diagnosis of Poisoning:
Diagnosis of poisoning is important, not only from therapeutic perspective but also
from legal aspects. The fast investigation regarding identification, dosage and route
of administration of the poison helps in better application of therapeutic measures.
Saving the patient’s life is a physician’s prime concern; additionally, the purpose of
poisoning - whether accidental, suicidal or homicidal - should be investigated.
a) Acute poisoning:
Manifestation of signs & symptoms is within a short time and attains complicated
features.
General symptoms of acute poisoning: Vomiting, Diarrhoea, Convulsions, Fainting,
Acute colic, Borborygmi, Excessive salivation, Deformed pupils,
Buzzing in the ears, Hyperthermia, Sweating, Delirium,
Neurological symptoms, Bluish discolouration, Anxiety,
Respiratory distress, Coldness of body-parts, Restlessness
b) Chronic poisoning:
Signs & symptoms develop gradually and at times remain concealed.
Sometimes the course of chronic poisoning is so slow that its signs & symptoms
represent themselves very mildly or as symptoms of another disease. Due to the
mildness, diagnosis of chronic poisoning is completely missed.
Common symptoms of chronic poisoning: Ill-being, Restlessness, Anxiety, Weakness,
Loss of weight, On & off presentation of gastro-intestinal symptoms
b) Ventilation
- Any crowd of people should be removed.
- Room should be well ventilated.
- Clothes of the patients should be loosened.
- Artificial or supportive respiratory measures
c) Treatment of hypotension
- If the systolic blood pressure falls below 99 mmHg, then the physician should
immediately arrange for artificial respiratory measures.
- Head-low position of patient
- Dopamine injection to enhance renal blood flow if required.
A) Contact poisons – Wash the area with clean water; Use of antidote if the
poison is known.
B) Inhaled poisons – Shifting the patient to fresh air; Sufficient ventilation;
Artificial respiration
C) Injected poisons – Application of tourniquet near the site of injection;
Application of ice packs; Incision & suction
D) Ingested poisons – Induction of vomiting; Gastric lavage
a) Induction of vomiting
- Indicated during the initial few (5-6) hours of ingestion of poison.
- Contraindicated in case of corrosive poisons, unconsciousness, children,
pregnancy
- Commonly used emetic drugs / agents:
▪ Ipecac powder (1-2 gm) in one glass water
▪ Ipecac syrup (30 ml)
▪ Zinc sulphate (1-2 gm) in one glass water
▪ Ammonium carbonate (1-2 gm) in one glass water
b) Gastric lavage (stomach wash)
- Gastric lavage is washing away of upper part of gastric tract for the removal
of ingested poisons.
- Gastric lavage tube / Boa’s tube / Ewald’s tube:
It is a rubber tube; length = 1 – 1.5 m; breadth = 12.7 mm
- For children = Ryle’s tube
- Indicated in ingested poisoning
- Contraindicated in case of corrosive poisoning, convulsions,
comatose patient, upper alimentary tract illness
iii) Antidotes:
- Antidotes are the substances that counteract or neutralize the effects of poisons.
- Types = Mechanical / Physical; Chemical; Physiological; Universal
Universal antidote:
Charcoal + Magnesium oxide (MgO) + Tannic acid
Ratio = 2:1:1
▪ Taking care of legal proceedings. The physician should not the name, address, sex,
age, occupation, date & time of arrival, accompanying members and complete
history of the patient. In case of a dying patient, the dying declaration should be
noted immediately.
▪ In case of sudden or accidental poisoning, if the physician feels that there can be a
mass poisoning, then he should promptly inform the concerned authorities about the
same.
▪ The patient should be immediately removed from the location of poisoning and it is
always judicious to admit him in a hospital.
▪ All the documents and evidences carefully preserved. Gastric contents, vomitus,
fecal matter, blood samples, etc. should be stored in containers and appropriately
labeled.
Visha Yoni
Classification of Visha on the basis of its source / origin:
D) According to Rasatarangini
Visha Vargikarana
Yoni / Utpatti Bheda
Refer to Visha Yoni
Prabhava Bheda
Classification of Visha on the basis of its effect:
A) Based on Karma:
i) Dahaka (Corrosives)
ii) Kshobhaka (Irritants)
iii) Vataprakopaka (Neurotics)
a) Mastishka prabhavaka (Cerebral poisons)
b) Hridaya prabhavaka (Cardiac poisons)
c) Phuphus prabhavaka (Pulmonary poisons)
d) Mahasrotas prabhavaka (GIT poisons)
e) Pranastha-nadi prabhavaka (Peripheral poisons)
f) Sushumna prabhavaka (Spinal poisons)
B) Based on Sthana:
i) Sthanika (Local)
ii) Sarvadaihika (General)
Adhisthana Bheda
Classification of Visha on the basis of its location:
A) Sthavara Adhisthana
i) Puspa (Flour)
ii) Phala (Fruit)
iii) Patra (Leave)
iv) Moola (Root)
v) Tvak (Bark)
vi) Beeja (Seeds)
vii) Kanda (Stem)
viii) Sara (Essence)
ix) Niryasa / Ksheera (Exudate / Latex)
x) Khanija (Metals / Minerals)
A) Jangama Adhisthana
i) Nishvasa (Exhalation) ix) Mukha (Mouth)
ii) Damstra (Teeth/Tusk) x) Sandamsha (Proboscis/Pincers)
iii) Nakha (Claws) xi) Vishardhita (Flatus)
iv) Mutra (Urine) xii) Tunda (Beak)
v) Purisha (Feaces) xiii) Asthi (Bones)
vi) Shukra (Semen) xiv) Pitta (Bile)
vii) Lala (Saliva) xv) Shuka (Bristles/Hair)
viii) Artava (Menstrual blood) xvi) Shava (Cadaver)
Visha – Madya – Ojas Guna
"लघु रूक्षमाशु ववशदुं व्यवावय तीक्ष्णुं ववकावस सूक्षुं च ।
उष्णमवनदे श्यरसुं दशगुणमु क्तुं ववषुं तज्ज्ै ैः ॥" (च् - वच – २३ / २४)
"लघूष्णतीक्ष्णसूक्ष्माम्लव्यवाय्याशुगमे व च ।
रूक्षुं ववकावश ववशदुं मद्युं दशगुणुं स्मततम् ॥ ३० ॥" (च - वच – २४ / ३०)
Jvara, Kasa, Shvasa, Hikka, Chardi, Trishna, Murccha, Anaha, Bastiruja, Shirashoola,
Shotha, Putidamshatva, Raktasrava, Vataprakopa, etc.
(Astanga Sangraha, Uttara Sthana, 57)
Visha Pariksha
Methods for the diagnosis of Visha are as follows:
1. Agniparikshana
2. Panchbhautika parikshana
3. Pariksha of animals and birds
4. Bhautika parikshana
5. Lakshananusara parikshana
a. Lakshana of Sthavara and Jangama Visha
b. Lakshana according to mode of administration
c. Lakshana according to site of poison
d. Lakshana according to use of poisoned material
e. Lakshana of Garvisha & Dushivisha
6. Ashumrut parikshana
1. Agniparikshana
Poisoned materials burn with single point flame (not with normal spreading flame),
become like peacock’s neck, interrupted and slow emit flames of different colours
like rainbow, and gives out cracking sound. The emerged smoke has cadaveric smell.
2. Indriya parikshana
▪ Shabda parikshana: poisoned food burns making loud cracks.
▪ Sparsha parikshana: contact with poisoned food causes burning sensation and nails
falling of hands.
▪ Rupa parikshana: when cast into the fire, poisoned material acquires the colours of
peacock’s neck.
▪ Rasa parikshana: lack of its natural taste.
▪ Gandha parikshana: on burning poisoned material emits irritating fumes which
smells like a cadaver.
5. Lakshananusara parikshana
a. Lakshana of Sthavara and Jangama Visha
▪ Sthavara Visha: Jvara, Hikka, Dantaharsha, Galagraha, Phena, Vamana,
Aruchi, Shvasa, Murccha
▪ Jangama Visha: Nidra, Tandra, Klama, Daha, Paka, Lomaharshana, Shopha,
Atisara
6. Ashumrut parikshana
▪ External and internal findings (sings) confirms the diagnosis of poisoning. For the
homicidal purpose, poison was ingested with mixing in food materials. Black coloured
hands, legs, teeth and nails in the dead body confirms it.
▪ Improper posture, scattered cloths and the number of episodes of diarrhoea
occurred confirms death by Dhattura poisoning.
▪ Discharge of blood from bite site, indicates snake bite.
▪ Food materials found in the dead was subjected to birds for the confirmation of the
poisoning.
Visha Data Lakshana
Visha Data Lakshana are the features of the person who intends to poison or
poisoned food, drinks, etc.
3. Chromatographic screenings
These methods are used for qualitative as well as quantitative determination of the
poison in the suspected samples. These are highly specific and fast acting techniques.
These can be used as corroborative evidence. These include followings:
a) Thin Layer Chromatography (TLC): This is only a qualitative test. This is very useful
in emergency to diagnose presence or absence of poison.
b) Liquid Chromatography (LC)
c) Gas Liquid Chromatography (GLC)
LC & GLC techniques are used for identification and quantification of solid, liquid as
well as gaseous poisons. GLC is preferably used for analysis of volatile and thermo-
stable pesticides, e.g., organophosphates, organochlorides, etc.
d) High Performance Liquid Chromatography (HPLC): With the help of this technique
minute traces of organic components of various mixtures can be separated and
analyzed. This is widely used for qualitative and quantitative analysis of lipstick
smears, heroin amphetamine, LSD green, pesticides, herbicides, alcohols, snake
venoms, plant & animal poisons, etc.
4. Ultraviolet - visible Spectroscopy
This is a quick & inexpensive technique for qualitative and quantitative analysis of
drugs like barbiturates, benzodiazepines, morphine, tranquilizers, DDT, parathion,
strychnine, aconitene, etc.
7. Immunoassay
It is accepted as the most practical method for determination and measurement of
substances with high protein content and difficult to isolate. These are very simple
but rapid techniques which do not require any pre-treatment of samples. The
concentration of the suspected poison is measured by enzyme activity of the poison.
Insulin, barbiturate, benzodiazepine and opiate derivatives may be studied by this
method.
Environment:
Environment includes the surroundings or conditions in which a person, animal or plant
operates, including air, water, land, natural resources, flora, fauna, humans and their
interrelation.
Types of Environment:
- Natural environment
- Man-made environment
- Social environment
Toxicity:
Toxicity refers to the potential of a substance to produce an adverse or harmful effect on a
living organism.
A toxicant is an agent that can produce an adverse effect in a biological system, seriously
damaging its structure or function or causing death.
Toxins:
• Metals, therapeutic drugs, industrial chemicals, pollutants, pesticides, fuels,
herbicides and abused drugs (exogenous)
• Bacterial toxins, parasitic products, bile, hormones (endogenous)
• Substances that accumulate in the body producing toxicity, even accumulated
nutrients and drugs could be toxic (Toxicity depends on dose)
• Toxins cause several disorders and are also predisposing factors or component
causes of most of the diseases.
• Environmental toxins are cancer-causing chemicals and endocrine disruptors, both
human-made and naturally occurring, that can harm our health by disrupting
sensitive biological systems.
Environmental Toxicity:
Environmental Toxicology is a multidisciplinary field of science concerned with the study of
harmful effects of various chemical, biological and physical agents on living organisms.
There are many sources of environmental toxicity that can lead to the presence of toxicants
in our food, water and air.
Pollutants are the prime source for Environmental Toxicity.
Pollution:
Pollution may be defined as an addition of undesirable material into the environment as a
result of human activities.
A pollutant may be defined as a physical, chemical or biological substance, released into the
environment which is directly or indirectly harmful to human and other living organisms.
i) Air pollution: A major source of air pollution results from the burning of fossil fuels.
Vehicle and factory emissions are common sources of this type of air pollution. The burning
of fossil fuels contributes to the formation of smog, a dense layer of particulate matter that
hangs like a cloud over many major cities and industrial zones. Air pollution contributes to
respiratory problems such as asthma, lung cancer, chronic bronchitis, and other lung
ailments. Nitrogen and sulfur oxides in the air contribute to acid rain, which is a form of
precipitation with a lower (more acidic) pH than normal. Acid rain harms forests, species that
live in water bodies, and degrades outdoor statues, monuments, and buildings.
ii) Water pollution: A major source of water pollution is runoff from agricultural fields,
industrial sites, or urban areas. Runoff disrupts the water body's natural balance. For
example, agricultural runoff typically includes fertilizer or toxic chemicals. Fertilizer can
cause algal blooms (an explosive growth of algae), choking out other plants and decreasing
the amount of available oxygen necessary for the survival of other species. Raw sewage is
another type of water pollutant. When sewage gets into the drinking water supply, serious
stomach and digestive issues may result, including the spread of diseases such as typhoid or
dysentery. A third source of water pollution is trash. Improperly disposed of items, such as
plastic bags, fishing line, and other materials may accumulate in the water and lead to the
premature death of animals that get tangled within the garbage.
ii) Soil pollution: Soil can become polluted by industrial sources or the improper disposal of
toxic chemical substances. Common sources of soil pollution include asbestos, lead, PCBs,
and overuse of pesticides/herbicides. Additionally, various compounds get into the soil from
the atmosphere, for instance with precipitation water, as well as by wind activity or other
types of soil disturbances, and from surface water bodies and shallow groundwater flowing
through the soil. Humans can be affected by soil pollution through the inhalation of gases
emitted from soils moving upward, or through the inhalation of matter that is disturbed and
transported by the wind because of the various human activities on the ground. Soil
pollution may cause a variety of health problems, starting with headaches, nausea, fatigue,
skin rash, eye irritation and potentially resulting in more serious conditions like
neuromuscular blockage, kidney and liver damage and various forms of cancer.
iv) Radioactive pollution: Radioactive pollution is defined as the physical pollution of living
organisms and their environment as a result of release of radioactive substances into the
environment due to factors such as nuclear explosions, testing of nuclear weapons, handling
and disposal of radioactive waste.
v) Light pollution: Light pollution refers to the large amount of light produced by most urban
and other heavily-populated areas. Light pollution prevents citizens from seeing features of
the night sky and has also been shown to impede the migration patterns of birds and the
activities of nocturnal animals.
vi) Noise pollution: Noise pollution typically refers to human-made noises that are either
very loud or disruptive in manner. This type of pollution has been shown to impact the
movement of sea mammals, such as dolphins and whales and also impacts the nesting
success of birds.
Chemical Warfare:
- Chemical warfare (CW) is defined as warfare that involves using of toxic properties of
chemical substances as weapons / ammunitions.
- Use of toxins such as ricine, botulinum toxin, etc. fall under this category.
- Nearly seventy different chemicals are marked as weapons for chemical warfare.
- Among the Weapons of Mass Destruction (WMD), chemical warfare is probably one of the
most brutal created by mankind. CW agents are extremely toxic synthetic chemicals that can
be dispersed as a gas, liquid or aerosol or as agents adsorbed to particles to become a
powder.
- Ethyl bromoacetate and chloroacetone were used as chemical weapons during the First
World War.
Classification of CW Agents:
In general, classification in terms of physiological effects produced on humans by the CW
agents is as follows:
i) Nerve agents
ii) Vesicants (blistering agents)
iii) Bloods agents (cyanogenic agents)
iv) Choking agents (pulmonary agents)
v) Riot-control agents (tear gases)
vi) Psychomimetic agents
vii) Toxins
Nuclear Warfare:
- Nuclear warfare is a military battle or political stratagem in which nuclear weapons are
used to cause damage on the enemy.
- This kind of warfare can produce destruction in much shorter time-interval and have long
lasting effects.
- So far, two nuclear weapons have been used in the course of warfare, both by the United
States near the end of World War II.
i) August 6, 1945 a uranium gun-type device was detonated over Hiroshima, Japan.
ii) August 9, 1945 a plutonium implosion-type device was detonated over Nagasaki, Japan.
-> These two bombings killed nearly 125.000 individuals.
CHAPTER vI: vishopakrama
(charaka Samhita)
ववषोर्क्रम – These are the main therapeutic treatments for poisons which help to
slow down the poisonous effect & expel the poison from the body. These treatments
may work independently or as a supportive measure to cure the patient from Visha.
The following 24 ववषोर्क्रम have been described:
"मन्त्राररष्टोत्कतप नवनष्पीडनचू षणाविर्ररषेकाैः ।
अवगाहरक्तमोक्षणवमनववरे कोर्िानावन ॥ ३५ ॥
हृदयावरणाञ्जननस्यिू मले हौषिप्रशमनावन ।
प्रवतसारणुं प्रवतववषुं सुंज्ञासुंथर्थार्नुं ले र्ैः ॥ ३६ ॥
मत तसञ्जीवनमे व च ववुंशवतरे ते चतु वभप रविकाैः ।
स्युरुर्क्रमा यर्था ये यत्र योज्ाैः शृणु तर्था तान् ॥ ३७ ॥" (च - वच - २३ / ३५-३७)
-> Refer to Charaka Samhita, Chikitsa Sthana, Chapter 23 for detailed description.
Chapter vii: visha & Upavisha
Kareveera
Latin name: Nerium indicum (Shveta)
Cerebra thevetia (Pita)
Family: Apocynaceae
English name: Indian oleander
Synonyms: Hayari, Hayamara, Ashvamara, Ashvaha, Ashvaghna
Types: Shveta, Pita
Category: Hridaya prabhavaka (Cardiac poison)
Active principles: Neriodorin, Neiodorein, Karabin
Signs & Symptoms: Kostha tapa, Daruna shoola, Chardi, Atisara, Akshepa
Chitraka
Latin name: Plumbago zeylanica
Family: Plumbaginaceae
English name: Ceylon leadwort / White leadwort
Synonyms: Agnika, Deepaka, Ushana, Analanama
Types: Shveta, Rakta
Category: Kshobhaka prabhavaka (Irritant poison)
Active principles: Plumbagin
Signs & Symptoms: Dagda, Daha, Chardi, Atisara, Trishna
Fatal dose: Uncertain
Fatal period: Few days
Treatment: Gastric lavage, Demulcents, Symptomatic treatment
Post-mortem app.: Signs of gastro-enteritis, Congestion of internal organs
Medico-legal aspects: Abortifacient, Homicidal poisoning
Formulations: Arogyavardhini Vati, Chandraprabha Vati,
Chitrakadi Vati, Hemagarbha pottali Rasa
Eranda
Latin name: Ricinus communis
Family: Euphorbiaceae
English name: Castor plant
Synonyms: Panchangula, Deerghadanda, Chitrabeeja, Vatari
Category: Kshobhaka prabhavaka (Irritant poison)
Active principles: Ricin
Hritpatri
Latin name: Digitalis purpurea
Family: Scrophulariaceae
English name: Digitalis / Foxglove
Category: Hridaya prabhavaka (Cardiac poison)
Active principles: Digitoxin, Digitonin, Digoxin
Tambaku
Latin name: Nicotina tabacum
Family: Solanaceae
English name: Tobacco
Synonyms: Tamrapatra, Gucchapatra, Ksharapatra, Krimighna
Category: Hridaya prabhavaka (Cardiac poison)
Active principles: Nicotine
Cerbera Odollam
Latin name: Cerbera Odollam
Family: Apocynaceae
English name: Suicide tree / Pong-pong / Othalanga
Category: Cardiac poison
Active principles: Cerberin (alkaloid toxin)
Garavisha
Garavisha is artificial poison obtained by combination of various substances. It is
classified under Kritrima Visha by Acharaya Vagbhata and Acharya Sushruta, and
under Samyogaja Visha by Acharya Charaka.
The patient of Garavisha who is suffering from such Lakshana and several other
Upadrava, should be considered as one who has reached the fatal stage.
Garavisha Chikitsa:
- Vamana, Pathya-ahara
- Suvarna lehana to purify Hridaya.
- Lehana with Sharkara, Kshaudra, Tapya & Suvarna churna.
- Churna of Murva, Amrita, Nata, Kana, Patoli, Chavya, Chitraka, Vacha, Musta &
Vidanga with Takra / Ushnodaka / Mastu / Amlarasa
B) According to Charaka Samhita (Cha. Chi. 23/14)
Garavisha is the type of poison which is prepared artificially by the mixture of various
substances. It produces diseases. Since it takes some time for this type of poison to
get metabolized and to produce its toxic effects, it does not cause instantaneous
death of a person.
Dushivisha
Dushivisha is slow poison which gradually develops over time. It is classified under
Kritrima Visha by Acharaya Vagbhata. Acharya Sushruta has described it as a variety
or complication of Sthavara, Jangama or Kritriam Visha.
Dushivisha Lakshana:
Liquid stool of different colours, Raktadusti, Trishna, Aruchi, Murccha, Chardi, Gudga-
vak (stammering), Dushi-udara, Kesha patana
Dushivisha in Amashaya causes Kapha-Vata Roga.
Dushivisha in Pakvashaya causes Vata-Pitta Roga.
Dushivisha in Dhatu causes various complications.
Dushivisha Prakopa:
Dushivisha gets aggravated by direct breeze, uncooked eatables, coldness, cloudy
weather, sleep during day, unsuitable eatables.
Dushivishari Agada:
The medicine or antidote (Agada) which is known as Dushivishari controls the
Dushivisha and other poisons.
It is prepared by making Kalka from Pippali, Dhyamaka, Jatamaamsi, Lodhra, Ela,
Suvarchika, Kutannata, Nata, Kustha, Yastimadhu, Chandana and Gairika.
It should be taken with Madhu.
B) According to Sushruta Samhita
Poison, whether Sthavara, Jangama or Kritrima Visha, which has not gone out of the
body completely, that poison which is very old, inactivated by anti-poisonous drugs,
that which is evaporated partially by fire, wind and sun, that which by nature is poor
in its quality, that type of poison is known as Dushivisha (impotent / weak poison).
It is named so because it does not kill the person quickly and remains in the body for
many years, covered by Kapha.
Dushivisha Purvarupa:
Nidra, Gurutva, Vijrimbha, Vishleshaharsha-Avatha (looseness of joints), Angamarda,
Ajeerna, Aruchi, Mandalakotha, Moha, Dhatukshaya, Pada-Kara Shopha, Udara,
Chardi, Atisara, Vaivarnya, Murccha, Vishamajvara, Trishna, Unmada, Adhovata,
Shukrakshaya, Gadga-vak, Kustha, etc.
Dushivisha Chikitsa:
The person suffering from effects of Dushivisha should undergo Svedana, Vamana &
Virechana. Then he should be give Agada Aushadha.
Dushivisha Agada:
Pippali, Dhyamaka, Jatamamsi, Lodhra, Paripelava, Suvarchika, Sukshma-ela, Valaka,
Kanakagairika – these should be processed to Churna or Kvatha and administered
with Madhu.
Viruddha Ahara
Food substances which provoke the Doshas, but do not expel them out of the body
are known as Viruddha.
The person who takes Viruddha-Ahara should be subjected to either Shodhana or
Shamana karma with Dravya which have opposite Guna to the ingested Viruddha-
Ahara. (A.H. Su. 7)
- Dugdha should not be taken after the intake of Mulaka, Lashuna, Shigru, Arjaka,
Sumukha, Surasa, etc. because it may cause Kustha.
- Hingu patra should not be taken with Madhu and Dugdha because it may cause
Uparodha, Bala-Varna-Teja-Veerya Nasha, and other serious diseases which may lead
to death.
- Dugdha should not be taken with Amla Rasa such as: Amra, Amrataka, Matulunga,
Nikuccha, Karamarda, Mocha, Kapittha, Panasa, Dadima, Amalaka, etc.
- Dugdha should not be taken with Kangu, Vanaka, Kulattha, Masha, Nishpava, etc.
- Meat of Haritala (bird) fried with Sarshapa Taila is Ahita and leads to severe
aggravation of Pitta.
- Pippali prepared with Matsya and Kakamachi mixed with Madhu causes death.
- Ushna Madhu or intake of Madhu by a person afflicted with Ushna causes death.
▪ Modification of Viruddha:
Viruddha is modified and does not act contradictory in particular cases such as:
- Lashuna Ksheera Paka
- Mulaka Svarasa with Dugdha
- Madhu with Vamana Dravya
▪ Definition of Ahita:
All food and drugs which dislodge the Dosha from their proper place, but do not
expel them out of the body are to be regarded as Ahita (unwholesome).
▪ Viruddha Bheda: - 18
2) Kala Viruddha Intake of Sheeta & Ruksha Dravya in Sheeta Kala (Ritu).
Intake of Katu & Ushna Dravya in Ushna Kala (Ritu).
11) Krama Viruddha Intake of Ahara before his bowel or urinary bladder is
clear; or intake of Ahara when there is no appetite or
appetite is highly aggravated.
12) Parihara Viruddha Intake of Ushna Dravya after intake of pork, etc.
13) Upachara Viruddha Intake of Sheeta Dravya after intake of ghee, etc.
14) Paka Viruddha Intake of Ahara which is prepared with bad/rotten food,
frozen food or preparation process includes excessive
coldness or heat.
16) Hridaya Viruddha Intake of Ahara which is not pleasing to the Mana.
Viruddha Ahara does not produce any effect or only little effect in following cases:
- Satmyata Habitual intake
- Alpataya Less quantity
- Diptagni Strong digestive fire
- Taruna Youth / Young age
- Snigdha Who has taken oleation
- Vyayama Regular physical exercise
- Balavana Strong person
▪ Chikitsa
The diseases caused by Viruddha Ahara are managed by Virechana, Vamana,
Shamana and Purva Hitasevana (prophylaxis).
Food Adulteration
- An adulterant is a chemical substance which should not be contained within other
substances (e.g. food, beverages, and fuels) for legal or other reasons.
- The addition of adulterants is called adulteration.
- The word is appropriate only when the additions are unwanted by the recipient.
Otherwise the expression would be food additive.
- Adulterants when used in illicit drugs are called cutting agents, while deliberate
addition of toxic adulterants to food or other products for human consumption is
known as poisoning.
2) Incidental: Pesticide residues tin from can, droppings of rodents, larvae in foods
3) Metallic contamination: Arsenic from pesticides, lead from water, mercury from
effluent, from chemical industries, tins from cans
Ice cream
• Adulterant: Pepperonil, Ethylacetate, Butraldehyde, Nitrate, Washing powder, etc.
• Health hazard: Pepperonil is used as a pesticide and ethyl acetate causes diseases
affecting lungs, kidneys and heart
Coffee powder
• Adulterant: Tamarind seeds, chicory powder
• Health hazard: diarrhea, stomach disorders, giddiness and severe joint pain
b) Honey
- Take a tablespoon of honey and put it in a glass of water. If the honey dissolves,
then it is not pure. Pure honey should stay together as a solid when submerged in
water.
- Take a bit of honey and mix it with water. Then place four or five drops of vinegar
into the solution. If it turns foamy, the honey might have been adulterated with
gypsum.
- Scoop a bit of honey into a spoon and let it fall from the spoon. Honey with high
water content will fall quickly. Mature honey of good quality will stay on the spoon or
fall very slowly.
- Light a match and try to burn some of the honey. If it lights and burns, then it is
pure. Impure or low-quality honey often contains extra water that keeps it from
burning.
- Take some honey, mix it with water, and add a few drops of iodine. If the solution
turns blue, then the honey has been adulterated with some sort of starch or flour.
- Take a small piece of old, hard bread and submerge it in the honey. After removing
it 10 minutes later, if the bread is still hard, then the honey is pure. If there is a lot of
water in the honey, the bread will soften.
c) Coconut oil
Detection of other oils in coconut oil:
Coconut solidifies when cooled and this property can be used to check the
adulteration of other oils in it. Take a transparent glass and keep in the refrigerator.
After a few hours, the coconut layer will solidify and there will be a separate layer if it
has adulteration of other oils.
d) Sugar
Detection of chalk powder in sugar:
Take a glass of water and add a spoonful of sugar. Sugar will dissolve in water and
chalk powder being heavier will settle down.
e) Spices
Detection of colour in red chili powder:
Artificial colour will leave a streak the moment red chili powder is added to water
and the pure one will just float on the surface leaving no immediate streak.
▪ Classification:
1) Non-bacterial food poisoning a) Irrational consumption of food
b) Metallic contamination
c) Food allergy
b) Metallic contamination:
Metallic contamination of food articles is not uncommon. It generally occurs due to
cooking or storing food in copper, bronze, aluminum, and other metallic vessels.
Ready to cook food items, canned food articles, bottles used for storing fruit juices
and cold drinks, packaging of chocolates, etc. multiply the incidence of metallic
contamination of food.
c) Food allergy:
Some individuals are allergic to certain food articles. Ingestion of these food articles
causes immediate allergic reaction that is manifested through nausea, vomiting,
diarrhoea, transient joint swelling, arthralgia, urticarial, etc.
In some cases, laryngo-pharyngeal oedema and asthma-like attacks also occur.
Signs & Symptoms: Variaton from person to person and depending on the
causative agent.
General: Diarrhoea, Nausea, Vomiting, Headache, Fever,
Colic pain, Shivering, Malaise
Sarpa Visha
-> Refer to Agadatantra Journal
Snakes
Features of Non-poisonous Snakes:
- Scales on the head are large.
- Scales on the belly are small to moderately large in size and they fall short or
cover the whole belly.
- Round pupils.
- Fangs are short and solid.
- Teeth are numerous but small.
- Tail is not markedly compressed.
- Not nocturnal in nature.
- Bite marks – numerous teeth in a row.
Poisonous Snakes:
1) Elapid (Neurotoxic)
2) Viper (Vasculotoxic)
3) Sea Snakes (Myotoxic)
Antivenom
Antivenom, also known as antivenin, venom antiserum, and antivenom
immunoglobulin, is a medication made from antibodies that is used to treat
certain venomous bites and stings. Antivenoms are recommended only if there
is significant toxicity or a high risk of toxicity. It is given by injection.
Side effects may be severe. They include serum sickness, shortness of breath,
and allergic reactions including anaphylaxis. Antivenom is made by collecting
venom from the relevant animal and injecting small amounts of it into a
domestic animal. The antibodies that form are collected from the domestic
animal's blood and purified.
Vrishchika Visha
-> Refer to Agadatantra Journal
Scorpions
- There are more than 1250 species of scorpions.
- Scorpions are more poisonous than snakes.
- Scorpion venom is neurotoxic & hemotoxic.
Keeta Visha
- According to Acharya Charka, insects (Keetas) are called so because they are
procreated from the Keetas or waste products like stool and urine of the snakes.
- Acharya Sushruta has described Keeta in his treatise after the chapters on snakes
and rodents. According to definition, Keeta may or may not be seen with naked eye.
Therefore, they can even be interpreted as insects, worms and even microbes. The
Pada may be legs, flagella or cilia; it can even be a part of single cell itself. When
considering unicellular animals.
- Most of the Keeta are neurotoxic. Some are vasculotoxic and some causes allergies.
Origin of Keeta: Keeta are born from the putrefied urine, feaces, semen, eggs, and
cadaver of snakes.
Classification of Keeta:
A) According to Acharya Charka
i) Dooshivisha Keeta (Chronic poison)
ii) Pranahara Keeta (Acute fatal poison)
B) Acharya Sushruta
a) Based on Dosha:
i) Vatika
ii) Paittika
iii) Shaishmika
iv) Sannipataja
b) Based on origin:
i) Shukra (Semen)
ii) Vit (Feaces)
iii) Mutra (Urine)
iv) Puti (Cadaver)
v) Anda (Eggs)
b) Pranahara Keeta:
Expanding oedema, as it happens in snakebite, associated with strong odour and
bleeding. Pain, heaviness of the eyes, fainting and dyspnoea.
- Acharya Vagbhata said that in all types of Keeta Damsha, Karnika, Sopha, Jwara,
Kandu and Arochaka will be prominent.
- Vataja Visha:
Heart pain, pain in joints and bones, tremors, dyspnoea, colour of the skin becomes
black, stiffness.
- In Pittaja Visha:
Heart burn, loss of sensation, bitterness of mouth, muscle fatigue, tenderness of
tissues, red and yellow colour
- Kaphaja Visha:
Vomiting, anorexia, coldness, sweetness of mouth, salivation etc.
- Pittaja:
Sheeta parisheka, Sheeta veerya lepana
- Kaphaja:
Lekhana, Tikshna Svedan, Vamana
Luta Visha
Luta Visha (bit of venomous spider) is extremely severe, difficult to comprehend and
difficult to treat by a Mandabhuddhi Bhishak (physician with low intelligence).
Day Symptoms
1 Isat Kandu (mild itching), Kotha (rash), Avyakta (unmanifested)
2 Pravyakta rupa (more manifested), Kotha is swollen in the peripheral area
and depressed in the center.
3 Rupa darshana (clearly manifested)
4 Kopa (aggravation)
5 Visha prakopaja vikara (diseases due to poison)
6 Prasara (dispersion), Avarana (enveloping) of marma-pradesha
7 Atipravriddha (severely aggravated), Whole body is afflicted, Mrityu (death)
Induction Symptoms
i) Shvasa Shotha with Jvara & Daha
(Breath)
ii) Damstra Vivarna, Kathina, Sthira, Gambhira Shopha, Toda, Vedana, Daha
(Bite / Sting)
iii) Shakrit Shopha, Durgandha, Daha, Kandu, Chimichima (tingling sensation),
(Feaces) Ashu pachana (quick ripening), Pandu varna (when pakva avastha)
Treatment:
- Nasya, Anjana, Abhyanga, Pana, Dhumapana, Avapidana, Kavala, Vamana,
Virechana, Raktamokshana
- In all kinds of Luta Visha, Shleshmataka Tvak and Akshiva-pippala should be
administered.
- Useful Dravya: Arkaparni, Karpasa, Raktachandana, Shaivala, Sariva,
Svarnaksheeri, Tvak, Vaikamkata, Hribera
- Pralepa with Manjistha, Gajakeshara, Patra, Rajani
- Alepa with Rajani, Daruharidra, Pattanga, Manjistha, Nagakeshara,
Sheetambu
Spiders
- Spider venoms are either cytotoxic or neurotoxic.
- Spider bite is known as arachnidism.
Signs & Symptoms: Localized swelling, pain & redness, Muscle cramps,
Delirium, Convulsions
Rat-bite Fever
Rat-bite fever is a disease caused by infected rodents.
Signs & Symptoms: Fever with chills, Arthralgia, Rash, Redness & swelling
at the site of bite, Lymphadenopathy near the site
of bite
Carbolic Acid
-> Refer to Agadatantra Journal
Sulphuric Acid
Chemical Formula: H2SO4
Synonym: Oil of Vitrol
Type: Inorganic acid
Physical appearance: Heavy, oily, colourless, non-fuming
Signs & Symptoms: Swollen tongue with white coating, Chalky white teeth,
Swollen & exfoliated lips, Severe burning sensation in
the oral cavity, Dysphagia, Epigastric pain, Brown / Black
vomit, Brown / Black streaks over the cheeks, chin, etc.;
Signs & Symptoms: Irritation of larynx & air passages, Salivation, Convulsion,
Delirium, Paralysis, Nausea, Epigastric pain
Nitric Acid
Chemical Formula: HNO3
Synonym: Aqua forties
Type: Inorganic acid
Physical appearance: Clear, colourless, fuming, heavy liquid; choking odour
Signs & Symptoms: Most rapid of all the poisons, Loss of consciousness,
Respiratory arrest
Oxalic Acid
Chemical Formula: C2H2O4
Synonym: Acid of sugar
Type: Organic acid
Physical appearance: Colourless, odourless, prismatic crystals, bitter taste
Alkalis
Commonly used: Ammonium hydroxide, Sodium carbonate, Potassium
carbonate, Sodium hydroxide, Potassium hydroxide
Mercury
Sanskrit Name = Parada
English Name = Mercury
Latin Name = Hydrargyrum
Symbol = Hg
Atomic Number = 80
Atomic weight = 200.6
Specific gravity = 13.6
Boiling point = 357°C
Freezing point = -39°C
Tin
Sanskrit Name = Vanga
English Name = Tin
Latin Name = Stannum
Symbol = Sn
Atomic Number = 50
Atomic weight = 118.7
Specific gravity = 7.3
Melting point = 232°C
Boiling point = 270.2°C
Fatal dose: 5 gm
Fatal period: 24 hrs
Treatment: Stomach wash, Purgatives, Demulcents, Symptomatic
treatment, Bala & Haritaki with Sitopala for 3 days
Phosphorus
Chemical Formula: P4
Type: Inorganic
Varieties: White / Crystalline, Red / Amorphous
Physical appearance: White: Waxy, crystalline, solid, garlicky odour
Red: Reddish-brown, amorphous, odourless
Carbon Dioxide
-> Refer to Agadatantra Journal
Carbon Monoxide
Chemical Formula: CO
Appearance: Colourless, odourless, tasteless, non-irritating gas
Post-mortem app.: Bright cherry-red skin & viscera, Froth from mouth &
nose, Hemorrhages in lungs, heart, brain, GIT
Hydrogen Sulphide
Chemical Formula: H2S
Appearance: Colourless, heavy, rotten egg-like smell, flammable gas
Household Poisons
1) Domestic household poisons: Boric acid, DDT, Naphthalene, Lead (toys),
Arsenic-copper-lead (crayons), Antimony
(matches), Zinc phosphide (rate paste),
Acetone (nail polish remover), sodium
hydroxide (drain cleaner), turpentine
(furniture polish), Kerosene (fuel), etc.
D.D.T. - Dichlorodiphenyltrichloroethane
Appearance: White, crystalline powder with aromatic odour,
almost insoluble in water
Signs & Symptoms: D.D.T. acts chiefly on the cerebellum and motor cortex.
Salivation, Nausea, Vomiting, Abdominal pain, Irritation
of eyes, nose and throat, Dilated pupils, Blurred vision,
Cough, Pulmonary oedema, Incoordination, Tremors,
Spasms, Convulsions, Paralysis, Collapse, Cyanosis,
Laboured respiration
Chronic toxicity: Anorexia, Emaciation, Anemia,
Liver & kidney damage
Aluminum Phosphate
Aluminum Phosphate is an odourless, white crystalline solid which is often used in
liquid or gel form. It is used in ceramics, dental cements, cosmetics, paints, paper and
pharmaceuticals.
Signs & Symptoms: Contact can irritate and burn the skin and eyes.
Inhaling Aluminum Phosphate can irritate the nose,
throat and lungs.
First Aid:
Eye Contact: Immediately flush with large amounts of cool water. Continue for
at least 15 minutes, occasionally lifting upper and lower lids. Remove contact
lenses, if worn, while rinsing. Immediate medical attention is necessary.
Skin Contact: Quickly remove contaminated clothing. Immediately wash
contaminated skin with large amounts of soap and water.
Inhalation: Remove the person from exposure. Begin rescue breathing (using
universal precautions) if breathing has stopped and CPR if heart action has
stopped. Transfer promptly to a medical facility.
CHAPTER xi: madya & madatyaya
Alcohol
Alcohol is a colourless, volatile flammable liquid which is produced by the natural
fermentation of sugars.
The term alcohol originally refers to ethanol, the intoxicating constituent in alcoholic
beverages such as spirits, wine, champagne and beer.
It is classified as a CNS Depressant.
General signs:
- Loss of self-control
- Inability to perform duties
- Danger to himself and others
Diagnosis:
i) Walk-and-Turn Test
ii) Horizontal Nystagmus Test (HGN)
iii) One-leg Stand Test
iv) Romberg Balance Test
v) Finger-to-Nose Test
When a person consumes alcohol, the full effects may take some time to become apparent.
Depending on a number of factors such as: Consumed amount, rate of consumption, gender,
body weight, empty or full stomach; there are somewhat predictable stages of alcohol
intoxication through which the individual may progress as their drinking continues.
Stage 1: Sobriety (Subclinical Intoxication)
Stage 2: Euphoria
Stage 3: Excitement
Stage 4: Confusion
Stage 5: Stupor
Stage 6: Coma
Stage 7: Death
Stage 2: Euphoria
The second stage of intoxication, referred to as euphoria, occurs between 0.03-0.12 BAC
(which may correspond to roughly 1-4 drinks for a woman or 2-5 for a man, depending on
size).
In this stage, the individual may feel more confident, may be more talkative and animated,
and may feel slightly euphoric. Inhibitions also begin to decline. Most people refer to this
stage as being “tipsy”.
While many of the effects of alcohol may be pleasurable to the drinker, the negative effects
of alcohol, such as impaired judgment, memory, and coordination begin to appear at this
time, as well. In this stage, a person’s motor responses may be significantly more delayed
than at a lower BAC.
Stage 3: Excitement
Having a BAC between 0.09-0.25. The individual may begin to experience emotional
instability, a lack of critical judgment, and a significant delay in reaction time. Slurred speech,
impaired perception and memory may also occur. Loss of balance. Drowsiness. Nausea and
vomiting.
Those around the person will likely notice that he / she is visibly drunk.
Stage 4: Confusion
Someone with a BAC level of 0.18 to 0.30 is in the confusion stage, characterized by
emotional upheaval and disorientation. Coordination is markedly impaired, to the extent
that the person may not be able to stand up, may stagger if walking, and may be very dizzy.
Those in this stage of intoxication are highly likely to forget things that happen to or around
them. “Blacking out” (losing memory of events that occurred while drinking) without actually
passing out can happen at this stage. In addition, a person may have and markedly increased
pain threshold, meaning they could injure themselves and not feel the effects until later.
Stage 5: Stupor
Stupor can occur at a BAC between approximately 0.25 and 0.40. Someone in this stage is
extremely intoxicated and in dangerous territory, as they are at great risk of alcohol
poisoning and death. They have likely lost a significant amount of motor function, are not
responding to stimuli (or responding very slowly) and may be unable to stand or walk,
stuporous or completely passed out, unable to voluntarily control certain bodily functions,
vomiting.
Someone in this stage should get medical help. Individuals left to “sleep it off” may end up
suffering from slowed breathing or respiratory arrest or may choke on their own vomit.
Other risks include hypothermia, arrhythmia, and seizures.
Stage 6: Coma
A person who has reached 0.35-0.45 BAC is at significant risk of lapsing into a
coma. Respiration and circulation are severely depressed, motor response and reflexes are
markedly decreased, and the person’s body temperature drops. The person who has
reached this stage is at risk of death.
Stage 7: Death
At about 0.45 BAC or above, many are unable to sustain their vital life functions, and the risk
of respiratory arrest and death is significant. Death may also be possible at lower BACs.
Treatment for Acute Alcoholism:
- Patient must be kept warm to treat hypothermia.
- Patient is made to lie on the side to prevent aspiration.
- Gastric lavage with alkaline solution within 2 hours of ingestion.
- One litre of normal saline or 10% glucose with 15 units of insulin to check hypoglycemia.
- Thiamine 100 mg to prevent neuropathy.
- Respiratory support.
- Dialysis may be required.
Risk factors:
A number of factors can increase the risk of alcohol poisoning, including:
- Size & weight, Overall health, Individual tolerance level
- Recent food intake / Empty stomach
- Combination of alcohol with other drugs, Percentage of alcohol in the
consumed drinks, Rate and amount of alcohol consumption
Complications:
- An unconscious person should not be left alone. Alcohol poisoning affects the
way the gag reflex works, someone with alcohol poisoning may choke on his /
her own vomit and not be able to breathe.
- Severe dehydration. Vomiting can result in severe dehydration, leading to
dangerously low blood pressure and fast heart rate.
- Seizures. Blood sugar level may drop low enough to cause seizures.
- Hypothermia. Body temperature may drop so low that it leads to cardiac
arrest.
- Irregular heartbeat. Alcohol poisoning can cause the heart to beat irregularly
or even stop.
- Brain damage. Heavy drinking may cause irreversible brain damage.
- Death. Any of the issues above can lead to death.
Methanol Poisoning
- Methanol poisoning is a toxicity due to methanol.
The initial symptoms of methanol exposure are usually less severe than the
symptoms from the ingestion of a similar quantity of ethanol.
Once the initial symptoms have passed, a second set of symptoms arises, from
10-30 hours after the initial exposure, they may include:
- Blurring or complete loss of vision, acidosis
- Putaminal hemorrhages (uncommon but serious complication)
These symptoms result from the accumulation of toxic levels of formate in the
blood, and may progress to death by respiratory failure.
Treatment:
Methanol poisoning can be treated with fomepizole, or if unavailable, ethanol.
Ethanol is considered as antidote for methanol. Both drugs act to reduce the
action of alcohol dehydrogenase on methanol by means of competitive
inhibition. Ethanol, the active ingredient in alcoholic beverages, acts as a
competitive inhibitor by more effectively binding and saturating the alcohol
dehydrogenase enzyme in the liver, thus blocking the binding of methanol.
Methanol is excreted by the kidneys without being converted into the very
toxic metabolites formaldehyde and formic acid. Alcohol dehydrogenase
instead enzymatically converts ethanol to acetaldehyde, a much less toxic
organic molecule.
CHAPTER xiI: Important acts
The primary objective of the act is to ensure that the drugs and cosmetics sold in
India are safe, effective and conform to state quality standards.
The central and the state governments are charged with the responsibility of
providing the drug of desired quality to the patients. Therefore, it is essential to root
out adulterated, spurious and misbranded drugs from the market.
The term "drug" as defined in the act includes a wide variety of substance, diagnostic
and medical devices. The act defines "cosmetic" as any product that is meant to be
applied to the human body for the purpose of beautifying or cleansing. The definition
however excludes soaps. In 1964, the act was amended to include Ayurveda and
Unani drugs.
The Drugs and Cosmetics Rules, 1945 are the set of rules under the Drugs and
Cosmetics Act, 1940 which contains provisions for classification of drugs under given
schedules and there are guidelines for the storage, sale, display and prescription of
each schedule.
Spurious Drugs
A drug may be deemed as spurious in following cases:
- If it is imported under a name which belongs to another drug.
- If it is an imitation of, or a substitute for, another drug or resembles another drug in
a manner likely to deceive or bears upon it or upon its label or container the name of
another drug unless it is plainly and conspicuously marked so as to reveal its true
character and its lack of identity with such other drug.
- If the label or the container bears the name of an individual or company purporting
to be the manufacturer of the drug, which individual or company is fictitious does not
exist; or if it has been substituted wholly or in part by another drug or substance.
- If it purports to be the product of a manufacturer of whom it is not truly a product.
Misbranded Drugs
A drug may be deemed as misbranded in following cases:
- If it is coloured, coated, powdered or polished in such a way that any damage is
concealed.
- If it is made to appear of better or greater therapeutic value than it really is.
- If it is not labeled in the prescribed manner.
- If its label or container or anything accompanying the drug bears any statement,
design or device which makes any false claim for the drug or which gives false or
misleading information.
Pharmacy Act, 1948
In India there was no restriction to practise the profession of pharmacy. One could
practice this profession as any other profession. Persons, having no knowledge and
having no education in pharmacy or pharmaceutical chemistry or pharmacology,
were engaged in this profession. Hundreds of cases were brought to the notice of the
Government wherein the compounding, mixing, or dispensing of medicines was
being done by persons who were not adequately educated in this line. The system
was causing great harm to the health of people by wrong compounding, mixing or
dispensing. It was found necessary to enact a law for the regulation of the profession
and practice of pharmacy. To achieve this goal, the Pharmacy Act, 1948 was
introduced.
The Act allows the Government of India to control the sales, supply and distribution
of any drug in India. The government can set maximum selling price, maximum
quantity to be possessed by dealer and maximum quantity to be sold to one person.
The government can impose various restriction of sale.
The Act require any retailer to give a cash memorandum to the customer for any
purchase above ₹5, and in case the purchase is below ₹5 the retailer must give a
memo if the customer demands.
The violation of the Act carries a maximum of 3 years with or without fine. In case of
corporate violators, every director, manager, secretary, agent or other officer or
person concerned with the management may be prosecuted unless the offence
occurred without his/her knowledge.
Narcotic Drugs and Psychotropic Substances Act, 1985
The Narcotic Drugs and Psychotropic Substances (NDPS) Act, 1985 is an Act of the
Parliament of India that prohibits a person to produce/manufacture/cultivate,
possess, sell, purchase, transport, store, and/or consume any narcotic drug or
psychotropic substance.
The Act extends to the whole of India and it applies also to all Indian citizens outside
India and to all persons on ships and aircraft registered in India.
Anyone who contravenes the NDPS Act will face punishment based on the quantity
of the banned substance.
- where the contravention involves a small quantity, with rigorous imprisonment for
a term which may extend to 1 year, or with a fine which may extend to ₹10,000
(US$140) or both;
- where the contravention involves a quantity lesser than commercial quantity but
greater than a small quantity, with rigorous imprisonment for a term which may
extend to 10 years and with fine which may extend to ₹1 lakh (US$1,400);
India had no legislation regarding narcotics until 1985. Cannabis smoking in India has
been known since at least 2000 BC and is first mentioned in the Atharvaveda, which
dates back a few hundred years BC.
The Indian Hemp Drugs Commission, an Indo-British study of cannabis usage in India
appointed in 1893, found that the "moderate" use of hemp drugs was "practically
attended by no evil results at all", "produces no injurious effects on the mind" and
"no moral injury whatever".
Regarding "excessive" use of the drug, the Commission concluded that it "may
certainly be accepted as very injurious, though it must be admitted that in many
excessive consumers the injury is not clearly marked".
Cannabis and its derivatives (marijuana, hashish/charas and bhang) were legally sold
in India until 1985, and their recreational use was commonplace. Consumption of
cannabis was not seen as socially deviant behaviour, and was viewed as being similar
to the consumption of alcohol. Ganja and charas were considered by upper class
Indians as the poor man's intoxicant, although the rich consumed bhang during Holi.