Class explanation:
Piperacillin is a broad-spectrum penicillin antibiotic, while Tazobactam is a beta-lactamase inhibitor that prevents bacterial resistance. They enhance antibacterial efficacy against a wide range of infections.
Use:
treatment of moderate to severe bacterial infection
effective against gram+, gram- and anaerobic bacteria
Common side effects:
nausea
diarrhoea
rash
Adverse effects:
hypersensitivity reactions
clostridioides difficile-associated diarrhoea (a bacterial infection in the colon which causes diarrhoea)
liver enzyme abnormalities
Mechanism of action:
Piperacillin inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins, leading to bacterial lysis. Tazobactam protects Piperacillin from degradation by bacterial beta-lactamases, expanding its spectrum of activity.
Drug interactions
May increase the risk of bleeding when used with anticoagulants
Reduces renal clearance of methotrexate, increasing toxicity risk.
Can reduce the effectiveness of amino glycosides when mixed in the same IV solution.
System:
Immune system
Amoxicillin is a penicillin antibiotic. Broad spectrum antibiotic. Used to treat bacterial caused infections.
3 common side affects may include:
fever
diarrhoea
headache
Adverse effects:
super infection
(rare) crystalluria, tooth discolouration in children
black hairy tongue
nausea/ vomiting
anaemia
(rare) hepatitis, cholestatic jaundice
Mechanism of action: Antibiotics aim to be 'harmful' to invading organisms without harming the host. This is known as selective 'toxicity'.
Drug interactions: Can interact with medications such as warfarin, allopurinol and probenecid. Could affect the stability of anticoagulant control. etc.
System: Immune system
Class: Gentamicin is a Aminoglycosides drug which is a class of antibiotics that are used to treat serious bacterial infections.
Use:
- infections of external eye
- life threatening infections where other antibacterial agents are ineffective or contraindicated
- soft tissue infection
Side effects:
- Rash
- diarrhoea
- Nausea
Adverse effects:
- Urticaria
- Ototocicity
- Increased or decreased urinary frequency
Drug interaction:
- NSAIDs
- Furosmide
System
Gram negative
- Anaesthetivs
Aciclovir is classified as a Anitviral drug because it stops the spread of herpes
use: of Aciclovir is treatment for herpes, simplex infections including type 1 & 2 herpes, shingles and advanced HIV diseases
Side effects: vertigo, headache, fatigue
adverse effects: renal damage, reversible abnormal liver enzymes and bilirubin, Hypotension
the action of Aciclovir is selectively taken up by herpes virus infected cell where it is converted to an active form that inhibits viral replication by interfering with DNA synthesis
drug interactions: cautions if use with mycophenolate mofetil, ciclosporin or tracrolimus. Not recomended with nephrotoic agents
System: the immune system
Why it belongs in class
work to inhibit viral replication which essential to control and treat viral infections
3 Common Side effects
Altered Tase
Diarrhea
Muscle pain
Adverse effects
Liver toxicity
Kidney impairment
Potential HIV Drug Resistance
Mechanisms of action
Nirmatrelvir + Ritonavir work by blocking virus replication and help the body fight off the infection faster
Drug Interactions
Avoid: Blood thinners (risk of heavy bleeding), heart meds (can affect heart rhythm) , cholesterol meds (Risk of muscle damage) , sedatives (Can cause extreme drowsiness) and transplant meds (reach extreme toxic levels).
Use with altered dose changes: Blood pressure meds, steroid and birth control pills
Body System
Digestive / Endocrine System
Tramadol is classified as an analgesic drug as it is primarily used to relieve pain.
USE:Commonly used to treat moderate to serve pain. eg. post surgical pain , injury related pain, chronic pain conditions, etc
COMMON SIDE EFFECTS:
1- NAUSEA
2- DIZZINESS
3- FATIGUE
ADVERSE EFFECTS:
1- RESPIRATORY DEPRESSION
2-SEIZURES
3- ADDICTION
MECHANISM OF ACTION:
Tramadol alters the way the brain and nervous system process/respond to pain, by binding opioid receptors in the brain and spinal cord, which helps reduce the perception of pain.
DRUG INTERACTION:
Tramadol can interact with blood-thinning medications like warfarin, potentially increasing the risk of bleeding.
SYSTEM: NERVOUS SYSTEM
Tapentadol is a pain-relieving medication that belongs to a class called analgesics. It works in two ways: like an opioid, it binds to receptors in the brain and spinal cord to reduce pain. Second, it inhibits the reuptake of norepinephrine, a chemical that helps control pain signals in the body. This dual action makes tapentadol effective for treating moderate to severe pain.
Use:
Chronic pain
Post surgical pain
3 Common side effects:
Dizziness, constipation, nausea.
Adverse effects:
Respiratory depression, low blood pressure, allergic reactions (rash, swelling)
Mechanism of Action:
It increases the levels of norepinephrine, a neurotransmitter, in the spinal cord, which helps to reduce pain by altering the way pain signals are transmitted. And it binds to a part of the brain called the mu-opioid receptor, which helps reduce pain.
Drug interactions:
increased risk of serotonin syndrome if given with serotoninergic agents such as SSNIs, SNRIs, TCAs, MAOIs or triptans
increased risk of respiratory depression if given with neuromuscular blocking agent or benzodiazepines
System:
Central Nervous System
Class: Opioid Analgesic
Explanation: Fentanyl is a synthetic opioid analgesic, classified under narcotics due to its potency in pain relief by acting on the opioid receptors in the brain.
Use: Used for the management of severe pain, including cancer pain, and for anaesthesia purposes.
3 Side Effects:
Drowsiness, Nausea, Constipation
3 Adverse Effects:
Respiratory depression, Hypotension & Risk of addiction.
Mechanism of Action: Fentanyl binds to the μ-opioid receptors in the brain and spinal cord, leading to analgesia and sedation by inhibiting pain transmission and respiratory function.
Drug Interactions: Interacts with CNS depressants (e.g., benzodiazepines, alcohol) which increases the risk of respiratory depression & overdose.
System: Central Nervous System (CNS)
Ramipril is a medication that belongs to a class of drugs called angiotensin-converting enzyme (ACE) inhibitors. It is commonly used to treat high blood pressure (hypertension) and heart failure. Additionally, it can help improve survival after a heart attack and reduce the risk of stroke and kidney problems in people with certain conditions.
3 common side effects are:
-Dizziness
-Cough
-Fatigue
-Headaches
Adverse Effects:
-Muscle spasms
-Cramps
-Myalgia
Mechanism of Action:
Ramipril is an angiotensin-converting enzyme (ACE) inhibitor. It works by blocking a substance in the body that causes blood vessels to tighten. As a result, ramipril relaxes the blood vessels. This lowers blood pressure and increases the supply of blood and oxygen to the heart.
Drug Interactions:
contraindicated with angiotensin II receptor antagonists in patients with diabetic nephropathy and not recommended in other patients taking angiotensin II receptor antagonists
• serum potassium may increase if given with heparin
• see General Interactions of ACE inhibitors
System:
-Cardiovascular System
Amitriptyline is an antidepressant, that works by increasing brain chemicals like serotonin and norepinephrine. While it's effective for depression, it’s less commonly used now due to side effects, with newer medications being preferred for treating depression.
amitriptyline is used for to treat chronic pain, depression, migraines, anxiety ,insomnia and tension headache by balancing brain chemical.
3 common side effects for this medication are;
Drowsiness;
Dry mouth;
Weight gain:
Adverse effects
Suicidal Thoughts –
Cardiovascular Issues –
Amitriptyline works by increasing the serotonin levels and norepinephrine brain levels by inhibiting their reuptake, which helps improves mood and reduce symptoms of depression and anxiety, it also has anticholinergic effects (causing dry mouth, blurred vision, etc.) and blocks histamine and alpha-1 receptors, leading to sedative effects and potential blood pressure drops. These actions contribute to both its therapeutic effects and side effects.
Amitriptyline can interact with several drugs, including MAOIs (risk of serotonin syndrome), other antidepressants(increased side effects), anticholinergic drugs (enhanced side effects like dry mouth or blurred vision), and blood pressure medications (may increase the risk of low blood pressure). Always inform a healthcare provider about all medications being taken to avoid harmful interactions.
Amitriptyline is included in central system
classified as an antidepressant because it helps balance the levels of serotonin in the brain.
Use to treat several mental health conditions such as Major Depression, Anxiety, OCD, PTSD, Social anxiety and more.
Common side effects: Nausea, Insomnia, Headache.
Adverse effects: Suicidal thoughts and behaviour. Serotonin Syndrome.
Mechanism of actions: Selective serotonin and noradrenaline reuptake inhibitors that prolongs action of serotonin and noradrenaline at receptors sites.
Drug interaction: Other antidepressants can increase the risk of serotonin syndrome. Increase the risk of bleeding if given with NSAIDs such as aspirin or warfarin.
Its apart of the central nervous system as it helps adjust serotonin levels in the brain.
use: Treatment of DVT, is a blood thinner to prevent blood clots.
3 common side affects:
thrombocytopenia,thrombocytopenia, thrombocytopenia
mechanism of action:
combines with antithrombin III (heparin co-factor) inactivating factor X and inhibiting the conversion of prothrombin to thrombin
drug interaction
drug interaction:
• decreased anticoagulant effect when given with antihistamines, digoxin, ascorbic acid (vitamin C), nicotine or tetracyclines
• decreased prothrombin time may occur if given simultaneously with IV glyceryl trinitrate, therefore should be given with caution, especially when starting or stopping therapy
• increased risk of hypoprothrombinaemia if given with large doses of aspirin
system: circulatory system
Sodium Valproate is an anticonvulsant used for epilepsy and bipolar disorder.
Use:
Simple partial epilepsy
Tonic-clonic epilepsy
Mono or adjuvant therapy in partial epilepsy
Mania
Common side Effects:
Drowsiness
Vertigo
Nausea/Vomiting
Adverse effects:
Anorexia, diarrhoea, abdominal cramps, increased appetite and/or weight gain.
Transient hair loss nail/nail-bed disorder
Elevated liver enzymes
It is believed to increase GABA levels, while also blocking voltage-dependent sodium channels.
Its half life is 8-12 hrs.
Not advised to take with Carbapenem antibiotic
Increased risk of liver failure with salicylates such as asprin
Clozapine may result in increased serum levels
Neurological, can cause CNS depression.
Lignocaine is classified as a antiarrhythmic/ anaesthesia because it blocks sodium channels in the heart, stabilizing electrical activity and preventing abnormal rhythms.
use : Treats ventricular arrhythmias, especially post-heart attack, and is used in cardiac resuscitation (ALS protocols).
Common Side Effects: Dizziness, lightheadedness, numbness.
Adverse Effects: Hypotension, bradycardia, seizures (CNS toxicity).
Mechanism of Action: Blocks fast sodium channels in the heart, stabilizing electrical activity and suppressing abnormal rhythms.
Drug Interactions:- Beta-blockers, amiodarone, cimetidine can increase toxicity risk. lignocaine
- may be decreased by propranolol and metoprolol, increasing the risk of toxicity
System: Cardiovascular
Class: Antiarrhythmic agents
Use : ventricullar fibrillation, atrial flutter and fibrillation, severe tachyarrhythmias
3 common side effects : nausea, vomiting, constipation
Adverse effects : severe bradycardia, sleep disorders, facial flushing
Mechanism of actions : increases coronary blood flow by vasodilation
Drug Interactions : not recommended with calcium channel blockers due to increased bradycardia and risk of conduction disorders
System : Central Nervous System (CNS)
Celecoxib is a COX-2 inhibitor (anti-inflammatory) it prevents prostaglandin synthesis* with actions similar to other NSAIDs with analgesic (pain), antipyretic (fever) and anti-inflammatory activity
Uses:
osteoarthritis,
rheumatoid arthritis,
ankylosing spondylitis
primary dysmenorrhoea (menstrual cramps)
(short-term) pain management post-surgery or musculoskeletal/soft tissue injury
Adverse affects:
Abdo pain and GI upset
N,V&D
Dizziness and fatigue
Interactions :
Increased plasma levels with fluconazole
Renal impairment with ACE inhibitors
May decrease effects of ACE inhibitor, angiotensin receptor antagonist, thiazide diuretics and beta-adrenoceptor blocking agents
System: Musculoskeletal
Proton Pump Inhibitor - Reduces gastric acid secretion produced by your stomach.
-Use: Benign gastric and duodenal ulcers, Gastro-oesophageal reflux disease (GORD), to prevent and treat ulcers and bleeding ulcers, Gastrinoma, Helicobacter Pylori.
-Common Side Effects: Nausea, vomiting, diarrhoea, constipation, flatulence, abdominal pain, fundic gland polyps.
-Adverse Effect: Vitamin B12 deficiency, Interstitial nephritis, hypomagnesaemia, increased risk of osteoporosis and bone fracture
-MOA: Inhibits the enzyme H+ - K+ATPase in the parietal cells
-Drug interaction: Contraindicated when treating H. Pylori with Clarithromycin in those with liver impairment.
-System: GIS
Class: Antipsychotic
Use: Schizophrenia
Action:blocks dopamine receptoes, reducing ysmptoms like hallucinations and delusions. At the same time it blocks serotonin receptors which helps improve mood and reduces movement related side effects.
3 side effects: drowsiness
Dizziness
Dry mouth
3 adverse effects:
Uncontrollable muscle movements
Metabolic changes(such as weight gain)
Unstable BP
System: CNS(Central Nervous System)
Drug interactions:
Alcohol: Effects and Risk
Effects: Increases drowsiness and can cause extreme dizziness, confusion, and difficulty concentrating. It may also increase the risk of falls and accidents.
Antipsychotic
Used to treat schizophrenia and mania in bipolar disorder (short term). Can be used for behavioural disorders related to autism
Common side effects:
Difficulty moving
Headaches
Changes in appetite
Adverse effects:
Drooling
Rash, dry skin
Rhinorrhea (runny nose)
Mechanism of action:
It works by balancing the levels of dopamine and serotonin in your brain, substances that help regulate mood, behaviors, and thoughts.
Drug interactions:
Not recommended by with psychostimulants (e.g. methylphenidate) due to increased risk of extrapyramidal symptoms
System:
Central nervous system
Midazolam is classified under neurological medications because it acts on the central nervous system (CNS) to produce sedation, reduce anxiety, and control seizures by enhancing the inhibitory effects of GABA
Uses:
Makes people sleepy before surgery.
Reduces anxiety.
Stops seizures.
3 Common Side Effects:
Drowsiness
Dizziness
Slow thinking
Adverse Effect:
Respiratory depression, which can lead to difficulty breathing and require medical intervention.
Mechanism of Action:
Midazolam binds to GABA-A receptors in the CNS, increasing the effects of GABA, the primary inhibitory neurotransmitter. This leads to sedation, muscle relaxation, anticonvulsant effects, and reduced anxiety.
Drug Interactions:
Opioids & other CNS depressants (increased risk of respiratory depression).
Alcohol (enhanced sedation and risk of overdose).
Some antifungal & antibiotic medications (can increase midazolam levels).
System Affected:
Neurological System
Respiratory System
Class- Antiparkinsons Agent
Levodopa is converted into dopamine in the brain, and carbidopa stops it from converting too early, letting more reach the brain.
Use- Parkinson's disease to release symptoms
3 common side effects- nausea, dizziness and orthostatic hypotension (standing)
Adverse effects- hallucinations or psychosis
Mechanism of action-
Levodopa is converted to dopamine in the brain, replenishing dopamine levels which are low in Parkinson's disease.
Carbidopa blocks the enzyme that converts levodopa to dopamine outside the brain, allowing more levodopa to reach the brain.
Drug interactions-
MAO inhibitors (with serotonergic drugs) can cause serotonin syndrome.
Antipsychotics can antagonize dopaminergic effects, reducing effectiveness.
System involved- central nervous system
Class: Anxiolytic Drug
Use:
Reduce symptoms of anxiety
3 common side effects:
Drowsiness, fatigue, muscle weakness
Adverse effects:
Confusion, depression and dizziness
Mechanism of action:
Stimulates GABA (gamma amino butyric acid) in the central nervous system, suppressing brain activity and convulsions.
Drug interactions:
Alcohol, narcotics, ketoconazole
System:
CENTRAL NERVOUS SYSTEM
Class: Antimalarial / Immunosuppressant
Hydroxychloroquine sulphate belongs to the antimalarial class because it is used to treat and prevent malaria caused by Plasmodium parasites. It is also classified as an immunosuppressant due to its ability to modulate the immune system, making it helpful in managing autoimmune conditions.
Use:
Malaria: Used to prevent and treat malaria.
Autoimmune Diseases: Treats conditions like rheumatoid arthritis and lupus, reducing inflammation and controlling symptoms by suppressing the immune system.
3 Common Side Effects:
Nausea
Headache
Dizziness
Adverse Effects:
Retinal toxicity (damage to the retina, leading to vision problems with long-term use)
Heart problems, such as arrhythmias
Severe skin reactions (e.g., rashes or skin pigmentation changes)
Mechanism of Action:
Hydroxychloroquine works by interfering with the growth and reproduction of Plasmodium parasites in red blood cells, treating malaria. For autoimmune diseases, it reduces inflammation and prevents the immune system from attacking the body’s tissues by altering immune cell activity.
Drug Interactions:
Antacids and Cimetidine can increase the levels of hydroxychloroquine in the bloodstream, increasing the risk of side effects.
May interact with digoxin, increasing the risk of heart issues.
System:
Immune System: Modulates immune function to reduce inflammation and control autoimmune disease symptoms.
Infectious Diseases: Targets and eliminates malaria-causing parasites in the bloodstream.