This document contains several case studies of patients who were prescribed multiple medications. For each case study, it identifies potential drug-drug interactions between the prescribed medications based on their mechanisms and effects. It provides the management recommendations to address each interaction, such as using caution, monitoring for specific adverse effects, or considering dose adjustments. The goal is to evaluate prescriptions for drug interactions and determine suitable management approaches to address any safety risks.
The document discusses important drug-drug interactions, including their intensity, mechanism, and management. It defines drug-drug interactions as when taking two drugs together causes a change in one drug's effects on the body. Interactions can be pharmacodynamic, involving receptor-level or intracellular effects, or pharmacokinetic, altering a drug's absorption, distribution, metabolism, or excretion. The document provides examples of serious interactions to avoid or monitor closely, outlines approaches to minimizing interactions, and poses sample cases to identify and manage interactions.
03.03 management of patients on antiretroviral drugs changiDavid Ngogoyo
This document provides guidance on changing or stopping antiretroviral therapy (ART) in a rational manner. It describes the main reasons for altering a patient's ART regimen as drug toxicity, interactions, or treatment failure. It discusses how to diagnose and manage common adverse drug reactions and interactions. It emphasizes the importance of assessing adherence before changing a patient's failing regimen and consulting national treatment guidelines and experts when making decisions about second-line therapy.
Case Studies (Clinical Pharmacy Assignment)
Case Studies
Case Study 1. Drug Related Problem
Case Study 2. Alcohol Toxicity
Case Study 3. Patient Counseling
Case Study 4. Peptic Ulcer
Case Study 5. Drug and the Newborn
Case Study 6. Night time Anxiety
Case Study 7. Clostridium Difficile
Case Study 8. Epilepsy and Pregnancy
Case Study 9. Parkinsonism
Case Study 10. Treatment May Be Worse Than Condition
Anti tuberculosis drug - induced hepatitis – A Case Studyvelspharmd
This case report describes a 32-year-old male patient who developed hepatotoxicity after being administered first-line anti-tuberculosis drugs to treat pulmonary tuberculosis. The patient also had a history of heavy alcohol use. Laboratory tests showed elevated liver enzymes and abdominal ultrasound revealed grade IV fatty liver infiltration. The patient was diagnosed with anti-TB drug-induced hepatitis exacerbated by alcohol-induced liver damage. His condition improved after discontinuing the anti-TB medications and alcohol, receiving supportive care, and standard treatment. The case report discusses the risk of hepatotoxicity from anti-TB drugs and importance of considering patient risk factors like alcohol use.
Clozapine Tablets USP 25mg, 50mg and 100mg Taj Pharma: Uses, Side Effects, Interactions, Pictures, Warnings, Clozapine Dosage & Rx Info | Clozapine Uses, Side Effects Clozapine: Indications, Side Effects, Warnings, Clozapine -Drug Information –Taj Pharma, Clozapine dose Taj pharmaceuticals Clozapine interactions, Taj Pharmaceutical Clozapine contraindications, Clozapine price, Clozapine Taj Pharma Clozapine SmPC-Taj Pharma Stay connected to all updated on Clozapine Taj Pharmaceuticals Mumbai. Patient Information Leaflets, SmPC.
A 45-year-old female patient presented with facial puffiness, myalgia, increased tiredness, hoarseness of voice and headache. Lab investigations revealed hypothyroidism. She was diagnosed with hypothyroidism and prescribed levothyroxine, otilonium bromide, ranitidine, ferrous sulfate, and calcium. The pharmacist intervened to recommend changing the dosing interval between levothyroxine and calcium to 4 hours apart to maximize levothyroxine efficacy and monitoring serum TSH levels.
This document contains several case studies of patients who were prescribed multiple medications. For each case study, it identifies potential drug-drug interactions between the prescribed medications based on their mechanisms and effects. It provides the management recommendations to address each interaction, such as using caution, monitoring for specific adverse effects, or considering dose adjustments. The goal is to evaluate prescriptions for drug interactions and determine suitable management approaches to address any safety risks.
The document discusses important drug-drug interactions, including their intensity, mechanism, and management. It defines drug-drug interactions as when taking two drugs together causes a change in one drug's effects on the body. Interactions can be pharmacodynamic, involving receptor-level or intracellular effects, or pharmacokinetic, altering a drug's absorption, distribution, metabolism, or excretion. The document provides examples of serious interactions to avoid or monitor closely, outlines approaches to minimizing interactions, and poses sample cases to identify and manage interactions.
03.03 management of patients on antiretroviral drugs changiDavid Ngogoyo
This document provides guidance on changing or stopping antiretroviral therapy (ART) in a rational manner. It describes the main reasons for altering a patient's ART regimen as drug toxicity, interactions, or treatment failure. It discusses how to diagnose and manage common adverse drug reactions and interactions. It emphasizes the importance of assessing adherence before changing a patient's failing regimen and consulting national treatment guidelines and experts when making decisions about second-line therapy.
Case Studies (Clinical Pharmacy Assignment)
Case Studies
Case Study 1. Drug Related Problem
Case Study 2. Alcohol Toxicity
Case Study 3. Patient Counseling
Case Study 4. Peptic Ulcer
Case Study 5. Drug and the Newborn
Case Study 6. Night time Anxiety
Case Study 7. Clostridium Difficile
Case Study 8. Epilepsy and Pregnancy
Case Study 9. Parkinsonism
Case Study 10. Treatment May Be Worse Than Condition
Anti tuberculosis drug - induced hepatitis – A Case Studyvelspharmd
This case report describes a 32-year-old male patient who developed hepatotoxicity after being administered first-line anti-tuberculosis drugs to treat pulmonary tuberculosis. The patient also had a history of heavy alcohol use. Laboratory tests showed elevated liver enzymes and abdominal ultrasound revealed grade IV fatty liver infiltration. The patient was diagnosed with anti-TB drug-induced hepatitis exacerbated by alcohol-induced liver damage. His condition improved after discontinuing the anti-TB medications and alcohol, receiving supportive care, and standard treatment. The case report discusses the risk of hepatotoxicity from anti-TB drugs and importance of considering patient risk factors like alcohol use.
Clozapine Tablets USP 25mg, 50mg and 100mg Taj Pharma: Uses, Side Effects, Interactions, Pictures, Warnings, Clozapine Dosage & Rx Info | Clozapine Uses, Side Effects Clozapine: Indications, Side Effects, Warnings, Clozapine -Drug Information –Taj Pharma, Clozapine dose Taj pharmaceuticals Clozapine interactions, Taj Pharmaceutical Clozapine contraindications, Clozapine price, Clozapine Taj Pharma Clozapine SmPC-Taj Pharma Stay connected to all updated on Clozapine Taj Pharmaceuticals Mumbai. Patient Information Leaflets, SmPC.
A 45-year-old female patient presented with facial puffiness, myalgia, increased tiredness, hoarseness of voice and headache. Lab investigations revealed hypothyroidism. She was diagnosed with hypothyroidism and prescribed levothyroxine, otilonium bromide, ranitidine, ferrous sulfate, and calcium. The pharmacist intervened to recommend changing the dosing interval between levothyroxine and calcium to 4 hours apart to maximize levothyroxine efficacy and monitoring serum TSH levels.
This document provides a nursing student's response to a case study on medications for a patient named Mr. MP. It includes details of the medications, their uses, dosages, side effects and special considerations. It also lists potential problems related to the medications, assessments to monitor for side effects, and healthcare providers to collaborate with including the physician, respiratory therapist, pharmacist, and physical therapist. The student identifies risks of bleeding, infection, and falls and interventions like careful injections, hand washing, and fall precautions. Assessments include respiratory, cardiovascular and musculoskeletal exams.
1. A 35-year old male with type 1 diabetes was admitted with fever, cough, and breathlessness due to right lower lobe pneumonia.
2. Laboratory tests showed elevated HbA1c of 9.1% and fasting blood sugar of 205.5 mg/dl. Chest x-ray found right lower lobe lung consolidation.
3. He was treated with antibiotics, cough suppressants, diabetes medications, and inhalers. His symptoms improved and he was discharged on oral medications with instructions to follow up in one week.
This document discusses drug-induced liver injury (DILI) caused by anti-tuberculosis drugs. It notes that isoniazid, rifampicin, and pyrazinamide, which are essential first-line drugs for tuberculosis treatment, can all cause hepatotoxicity. It outlines the mechanisms of anti-TB drug toxicity including direct toxicity, idiosyncratic reactions, and enzyme induction. Risk factors for anti-TB DILI are described. Diagnosis involves criteria such as elevated liver enzymes and bilirubin levels as well as tools like the RUCAM scoring system. Management recommendations include monitoring liver function tests during treatment, criteria for stopping drugs, second-line drug regimens after stopping first
This document provides guidance on clinical pharmacology and safe prescribing practices. It discusses key considerations for prescribing medications including deciding if a drug is necessary, assessing risks and benefits, choosing a drug based on safety, efficacy and cost, taking an accurate drug history, prescribing accurately, educating patients, and improving compliance. It highlights important information to include when prescribing such as dose, route of administration, how to take the drug, and potential adverse reactions. The document emphasizes that prescribing requires responsibility to prevent harm and outlines responsibilities of physicians in relation to prescribing.
This document presents case presentations for hypertension, diabetes mellitus, and community acquired pneumonia for a patient named Pooja. It summarizes the subjective and objective findings, assessments, diagnoses, etiologies, need for therapy, and current medications for each condition. It also provides information on common electrolyte solutions, assessments of current antihypertensive, antidiabetic, antibiotic, and other supportive care therapies including generic and brand names, mechanisms of action, administrations, adverse effects and contraindications.
The document discusses pharmacovigilance and provides definitions and guidelines for reporting adverse drug reactions (ADRs). It describes how to fill out an ADR form, including a case example of a 59-year-old man who developed numbness and tingling due to metformin-induced vitamin B12 deficiency. It also reviews scales for assessing causality of ADRs, including the WHO causality scale and Naranjo algorithm. A second case example describes a patient who had a fixed drug eruption from levofloxacin with a history of prior reaction to the drug.
A 34-year-old female was admitted to the hospital presenting with auditory hallucinations, reduced sleep, irritability, and poor self-care for the past 3 years. Her lab work showed some abnormal results. She was diagnosed with undifferentiated schizophrenia. Her treatment plan included olanzapine, clonazepam, trihexyphenidyl, risperidone, propranolol, multivitamins, and lactulose. She showed some improvement in symptoms and was discharged on medications including risperidone, clonazepam, trihexyphenidyl, and propranolol.
Medication Administration Through Enternal Feeding TubesGerinorth
Based on the information provided:
- Ciprofloxacin absorption is decreased by 50% when taken with milk feeds
- Milk feeds should be withheld 1 hour before and 2 hours after administering ciprofloxacin
- The enteral feeds are given at 6am, 10am, 2pm, 6pm, 10pm
- To maximize absorption of ciprofloxacin, it should be administered at 9am and 7pm, allowing at least a 1 hour gap before and 2 hours after the enteral feeds.
This presentation summarizes key information about the drug amlodipine. It introduces amlodipine as a medication used to treat high blood pressure and coronary artery disease. The presentation outlines amlodipine's pharmacology as a calcium channel blocker, recommended dosages, dosage forms, contraindications, adverse effects, and drug-drug interactions. It also discusses amlodipine's pregnancy category, effects on breastfeeding, and important counseling points for patients.
This document discusses tuberculosis (TB) globally and in Pakistan. It notes that TB infects over 1 billion people worldwide and causes millions of deaths each year. Pakistan has a high burden of TB, ranking 8th globally. The document then covers diagnosis and treatment of TB, including different regimens for new cases, re-treatment cases, and special populations like pregnant women, infants, and those with renal impairment or HIV/AIDS. It discusses managing TB in patients with conditions like silicosis or hepatitis induced by anti-TB treatment. The goal is to provide guidance on treating TB in complex situations.
Drug Monograph and Literature Review: "Arcapta Neohaler"Joy Awoniyi
This document provides a drug monograph and literature review for Arcapta Neohaler, which contains indacaterol maleate. It is approved for the treatment of chronic obstructive pulmonary disease (COPD) as a once-daily long-acting beta agonist. The monograph details the drug's indications, dosage forms, mechanism of action, pharmacokinetics, contraindications, warnings, adverse effects, drug interactions, and dosing. It concludes with a review of the literature on indacaterol maleate and COPD treatment.
Fluorouracil 50mgml injection smpc taj pharmaceuticalsTaj Pharma
FLUOROURACIL Taj Pharma : Uses, Side Effects, Interactions, Pictures, Warnings, FLUOROURACIL Dosage & Rx Info | FLUOROURACIL Uses, Side Effects -: Indications, Side Effects, Warnings, FLUOROURACIL - Drug Information - Taj Pharma, FLUOROURACIL dose Taj pharmaceuticals FLUOROURACIL interactions, Taj Pharmaceutical FLUOROURACIL contraindications, FLUOROURACIL price, FLUOROURACIL Taj Pharma Cancer, oncologyFluorouracil 50mg/ml Injection. SMPC- Taj Pharma
1. The document discusses various important aspects of preventing and managing adverse drug reactions (ADRs) to anti-tuberculosis drugs, including monitoring patients, educating them, and recognizing and treating side effects early.
2. It identifies common ADRs caused by different anti-TB drugs like nausea, rash, hepatitis, peripheral neuropathy, and strategies for preventing and managing them.
3. Reporting all ADRs to the Pharmacovigilance Program of India is emphasized to monitor safety and improve treatment protocols.
Nln pharmacology study guide final 6 3-2013Dr P Deepak
This document provides guidance for studying for the NLN Pharmacology Exam. It outlines that the exam contains 100 multiple choice questions testing calculations, principles of medication administration, and medication effects. Approximately 1/3 of the exam focuses on calculations, so the guide emphasizes practicing dosage calculations and reviews common calculation methods. It also reviews key principles like the rights of medication administration, routes of drug administration, and definitions of important terms. The goal is to prepare nurses to demonstrate competency in safe medication administration.
Telaprevir is a protease inhibitor approved to treat genotype 1 chronic hepatitis C in
combination with peginterferon and ribavirin. It works by inhibiting the HCV NS3/4A protease
to prevent viral replication. Several clinical trials found telaprevir combination therapy resulted
in higher rates of undetectable HCV RNA levels and sustained virologic response compared to
peginterferon-ribavirin alone. The most common side effects were rash, pruritis, fatigue, and
gastrointestinal issues. Though telaprevir is associated with more side effects, its ability to
shorten treatment duration and improve outcomes outweighs the increased costs. As such, the
This document summarizes several new antiemetic treatments for chemotherapy-induced nausea and vomiting (CINV). It discusses studies on palonosetron, casopitant, olanzapine, midazolam, and gabapentin. Palonosetron was shown to be as effective as ondansetron for CINV from cisplatin and more effective than ondansetron/dolasetron for moderately emetogenic chemo. Casopitant and olanzapine show promise for controlling CINV when added to standard antiemetics. Midazolam helped reduce refractory acute CINV. Further research is still needed on the roles of these new antiemetics.
Fluconazole 150 mg capsule smpc taj pharmaceuticalsTaj Pharma
Fluconazole Taj Pharma : Uses, Side Effects, Interactions, Pictures, Warnings, Fluconazole Dosage & Rx Info | Fluconazole Uses, Side Effects -: Indications, Side Effects, Warnings, Fluconazole - Drug Information - Taj Pharma, Fluconazole dose Taj pharmaceuticals Fluconazole interactions, Taj Pharmaceutical Fluconazole contraindications, Fluconazole price, Fluconazole Taj Pharma Fluconazole 150 mg Capsule SMPC- Taj Pharma . Stay connected to all updated on Fluconazole Taj Pharmaceuticals Taj pharmaceuticals Hyderabad.
A 54-year-old woman was admitted to the hospital after vomiting blood and was found to have a bleeding duodenal ulcer. She received treatment including blood transfusion and endoscopic hemostasis. Testing showed infection with Helicobacter pylori. She is now well and ready for discharge. The doctor needs to prescribe treatment to eradicate H. pylori and prevent ulcer recurrence, as well as restart the patient's usual hypertension medications. A discharge letter will be provided to the general practitioner with details of treatment changes.
This document provides information on several medications including atropine, epinephrine, hydrocortisone, dopamine, furosemide, digoxin, digoxin immune fab, naloxone, phenytoin, phenobarbitone, and potassium chloride. For each medication, the document outlines indications, dosages, cautions, adverse effects, and monitoring as applicable. The document also provides treatment protocols for conditions like status asthmaticus and anaphylactic shock.
EVALUATION OF PRESCRIPTIONS GENERATED IN HOSPITAL FOR DRUG INTERACTIONS AND F...knight116
These were some of the prescriptions i've found in the hospital with interactions, these may be mild/moderate/severe. The interactions were minimised after they have been identified.
Case study on Paranoid Schizophrenia.pptxJeeva Anand
1) A 52-year-old female patient was admitted to the hospital complaining of talking to herself, suspiciousness, increased anger, irritability, reduced sleep, and reduced food intake over the past week.
2) She has a history of schizophrenia for over 22 years and has been admitted 6 times previously. She is currently on medications for schizophrenia, hypertension, and Parkinson's disease.
3) She was assessed as having paranoid schizophrenia based on delusions of persecution and a restricted affect. She was started on a treatment plan including olanzapine, lorazepam, haloperidol, clonazepam, and clozapine.
This document provides a nursing student's response to a case study on medications for a patient named Mr. MP. It includes details of the medications, their uses, dosages, side effects and special considerations. It also lists potential problems related to the medications, assessments to monitor for side effects, and healthcare providers to collaborate with including the physician, respiratory therapist, pharmacist, and physical therapist. The student identifies risks of bleeding, infection, and falls and interventions like careful injections, hand washing, and fall precautions. Assessments include respiratory, cardiovascular and musculoskeletal exams.
1. A 35-year old male with type 1 diabetes was admitted with fever, cough, and breathlessness due to right lower lobe pneumonia.
2. Laboratory tests showed elevated HbA1c of 9.1% and fasting blood sugar of 205.5 mg/dl. Chest x-ray found right lower lobe lung consolidation.
3. He was treated with antibiotics, cough suppressants, diabetes medications, and inhalers. His symptoms improved and he was discharged on oral medications with instructions to follow up in one week.
This document discusses drug-induced liver injury (DILI) caused by anti-tuberculosis drugs. It notes that isoniazid, rifampicin, and pyrazinamide, which are essential first-line drugs for tuberculosis treatment, can all cause hepatotoxicity. It outlines the mechanisms of anti-TB drug toxicity including direct toxicity, idiosyncratic reactions, and enzyme induction. Risk factors for anti-TB DILI are described. Diagnosis involves criteria such as elevated liver enzymes and bilirubin levels as well as tools like the RUCAM scoring system. Management recommendations include monitoring liver function tests during treatment, criteria for stopping drugs, second-line drug regimens after stopping first
This document provides guidance on clinical pharmacology and safe prescribing practices. It discusses key considerations for prescribing medications including deciding if a drug is necessary, assessing risks and benefits, choosing a drug based on safety, efficacy and cost, taking an accurate drug history, prescribing accurately, educating patients, and improving compliance. It highlights important information to include when prescribing such as dose, route of administration, how to take the drug, and potential adverse reactions. The document emphasizes that prescribing requires responsibility to prevent harm and outlines responsibilities of physicians in relation to prescribing.
This document presents case presentations for hypertension, diabetes mellitus, and community acquired pneumonia for a patient named Pooja. It summarizes the subjective and objective findings, assessments, diagnoses, etiologies, need for therapy, and current medications for each condition. It also provides information on common electrolyte solutions, assessments of current antihypertensive, antidiabetic, antibiotic, and other supportive care therapies including generic and brand names, mechanisms of action, administrations, adverse effects and contraindications.
The document discusses pharmacovigilance and provides definitions and guidelines for reporting adverse drug reactions (ADRs). It describes how to fill out an ADR form, including a case example of a 59-year-old man who developed numbness and tingling due to metformin-induced vitamin B12 deficiency. It also reviews scales for assessing causality of ADRs, including the WHO causality scale and Naranjo algorithm. A second case example describes a patient who had a fixed drug eruption from levofloxacin with a history of prior reaction to the drug.
A 34-year-old female was admitted to the hospital presenting with auditory hallucinations, reduced sleep, irritability, and poor self-care for the past 3 years. Her lab work showed some abnormal results. She was diagnosed with undifferentiated schizophrenia. Her treatment plan included olanzapine, clonazepam, trihexyphenidyl, risperidone, propranolol, multivitamins, and lactulose. She showed some improvement in symptoms and was discharged on medications including risperidone, clonazepam, trihexyphenidyl, and propranolol.
Medication Administration Through Enternal Feeding TubesGerinorth
Based on the information provided:
- Ciprofloxacin absorption is decreased by 50% when taken with milk feeds
- Milk feeds should be withheld 1 hour before and 2 hours after administering ciprofloxacin
- The enteral feeds are given at 6am, 10am, 2pm, 6pm, 10pm
- To maximize absorption of ciprofloxacin, it should be administered at 9am and 7pm, allowing at least a 1 hour gap before and 2 hours after the enteral feeds.
This presentation summarizes key information about the drug amlodipine. It introduces amlodipine as a medication used to treat high blood pressure and coronary artery disease. The presentation outlines amlodipine's pharmacology as a calcium channel blocker, recommended dosages, dosage forms, contraindications, adverse effects, and drug-drug interactions. It also discusses amlodipine's pregnancy category, effects on breastfeeding, and important counseling points for patients.
This document discusses tuberculosis (TB) globally and in Pakistan. It notes that TB infects over 1 billion people worldwide and causes millions of deaths each year. Pakistan has a high burden of TB, ranking 8th globally. The document then covers diagnosis and treatment of TB, including different regimens for new cases, re-treatment cases, and special populations like pregnant women, infants, and those with renal impairment or HIV/AIDS. It discusses managing TB in patients with conditions like silicosis or hepatitis induced by anti-TB treatment. The goal is to provide guidance on treating TB in complex situations.
Drug Monograph and Literature Review: "Arcapta Neohaler"Joy Awoniyi
This document provides a drug monograph and literature review for Arcapta Neohaler, which contains indacaterol maleate. It is approved for the treatment of chronic obstructive pulmonary disease (COPD) as a once-daily long-acting beta agonist. The monograph details the drug's indications, dosage forms, mechanism of action, pharmacokinetics, contraindications, warnings, adverse effects, drug interactions, and dosing. It concludes with a review of the literature on indacaterol maleate and COPD treatment.
Fluorouracil 50mgml injection smpc taj pharmaceuticalsTaj Pharma
FLUOROURACIL Taj Pharma : Uses, Side Effects, Interactions, Pictures, Warnings, FLUOROURACIL Dosage & Rx Info | FLUOROURACIL Uses, Side Effects -: Indications, Side Effects, Warnings, FLUOROURACIL - Drug Information - Taj Pharma, FLUOROURACIL dose Taj pharmaceuticals FLUOROURACIL interactions, Taj Pharmaceutical FLUOROURACIL contraindications, FLUOROURACIL price, FLUOROURACIL Taj Pharma Cancer, oncologyFluorouracil 50mg/ml Injection. SMPC- Taj Pharma
1. The document discusses various important aspects of preventing and managing adverse drug reactions (ADRs) to anti-tuberculosis drugs, including monitoring patients, educating them, and recognizing and treating side effects early.
2. It identifies common ADRs caused by different anti-TB drugs like nausea, rash, hepatitis, peripheral neuropathy, and strategies for preventing and managing them.
3. Reporting all ADRs to the Pharmacovigilance Program of India is emphasized to monitor safety and improve treatment protocols.
Nln pharmacology study guide final 6 3-2013Dr P Deepak
This document provides guidance for studying for the NLN Pharmacology Exam. It outlines that the exam contains 100 multiple choice questions testing calculations, principles of medication administration, and medication effects. Approximately 1/3 of the exam focuses on calculations, so the guide emphasizes practicing dosage calculations and reviews common calculation methods. It also reviews key principles like the rights of medication administration, routes of drug administration, and definitions of important terms. The goal is to prepare nurses to demonstrate competency in safe medication administration.
Telaprevir is a protease inhibitor approved to treat genotype 1 chronic hepatitis C in
combination with peginterferon and ribavirin. It works by inhibiting the HCV NS3/4A protease
to prevent viral replication. Several clinical trials found telaprevir combination therapy resulted
in higher rates of undetectable HCV RNA levels and sustained virologic response compared to
peginterferon-ribavirin alone. The most common side effects were rash, pruritis, fatigue, and
gastrointestinal issues. Though telaprevir is associated with more side effects, its ability to
shorten treatment duration and improve outcomes outweighs the increased costs. As such, the
This document summarizes several new antiemetic treatments for chemotherapy-induced nausea and vomiting (CINV). It discusses studies on palonosetron, casopitant, olanzapine, midazolam, and gabapentin. Palonosetron was shown to be as effective as ondansetron for CINV from cisplatin and more effective than ondansetron/dolasetron for moderately emetogenic chemo. Casopitant and olanzapine show promise for controlling CINV when added to standard antiemetics. Midazolam helped reduce refractory acute CINV. Further research is still needed on the roles of these new antiemetics.
Fluconazole 150 mg capsule smpc taj pharmaceuticalsTaj Pharma
Fluconazole Taj Pharma : Uses, Side Effects, Interactions, Pictures, Warnings, Fluconazole Dosage & Rx Info | Fluconazole Uses, Side Effects -: Indications, Side Effects, Warnings, Fluconazole - Drug Information - Taj Pharma, Fluconazole dose Taj pharmaceuticals Fluconazole interactions, Taj Pharmaceutical Fluconazole contraindications, Fluconazole price, Fluconazole Taj Pharma Fluconazole 150 mg Capsule SMPC- Taj Pharma . Stay connected to all updated on Fluconazole Taj Pharmaceuticals Taj pharmaceuticals Hyderabad.
A 54-year-old woman was admitted to the hospital after vomiting blood and was found to have a bleeding duodenal ulcer. She received treatment including blood transfusion and endoscopic hemostasis. Testing showed infection with Helicobacter pylori. She is now well and ready for discharge. The doctor needs to prescribe treatment to eradicate H. pylori and prevent ulcer recurrence, as well as restart the patient's usual hypertension medications. A discharge letter will be provided to the general practitioner with details of treatment changes.
This document provides information on several medications including atropine, epinephrine, hydrocortisone, dopamine, furosemide, digoxin, digoxin immune fab, naloxone, phenytoin, phenobarbitone, and potassium chloride. For each medication, the document outlines indications, dosages, cautions, adverse effects, and monitoring as applicable. The document also provides treatment protocols for conditions like status asthmaticus and anaphylactic shock.
EVALUATION OF PRESCRIPTIONS GENERATED IN HOSPITAL FOR DRUG INTERACTIONS AND F...knight116
These were some of the prescriptions i've found in the hospital with interactions, these may be mild/moderate/severe. The interactions were minimised after they have been identified.
Case study on Paranoid Schizophrenia.pptxJeeva Anand
1) A 52-year-old female patient was admitted to the hospital complaining of talking to herself, suspiciousness, increased anger, irritability, reduced sleep, and reduced food intake over the past week.
2) She has a history of schizophrenia for over 22 years and has been admitted 6 times previously. She is currently on medications for schizophrenia, hypertension, and Parkinson's disease.
3) She was assessed as having paranoid schizophrenia based on delusions of persecution and a restricted affect. She was started on a treatment plan including olanzapine, lorazepam, haloperidol, clonazepam, and clozapine.
Adrenergic drugs and there classificationNitin Vaidya
This document discusses different types of adrenergic drugs. It describes alpha and beta adrenergic blocking drugs, which are competitive antagonists that inhibit the receptor action of adrenaline. Specific drugs are discussed, including prazosin, terazosin, and doxazosin as selective alpha-1 blockers, and propranolol as a nonselective beta blocker. Their mechanisms of action, pharmacokinetics, uses, interactions and adverse effects are summarized. The document also mentions alpha/beta blockers like labetalol and carvedilol used to treat hypertension and congestive heart failure.
Pancreatitis is the Inflammation of the pancreatic parenchyma. Acute condition of diffuse pancreatic inflammation & auto digestion, presents with abdominal pain, and is usually associated with raised pancreatic enzyme levels in the blood &urine. this is a case study on acute pancreatitis describing factors such as patient demographic data , pharmacist intervention , pathophysiology , treatment , prevention , imaging techniques , diagnosis , lab investigation etc
this case study was prepared for my academic purpose ......
please comment .........
thank u,,,,,
Organophosphate Poisoning - Update on Management Anoop James
Organophosphorus compounds are widely used as pesticides and were also developed as nerve agents. They work by inhibiting the enzyme acetylcholinesterase, leading to excess acetylcholine in the body and cholinergic toxicity. Management of organophosphate poisoning involves atropinization to counteract effects, with incremental atropine dosing shown to be better than bolus dosing. While pralidoxime is recommended to reactivate acetylcholinesterase, clinical trials show no clear benefit and potential for harm. Three types of paralysis can occur - acute cholinergic crisis, intermediate syndrome, and organophosphate-induced delayed polyneuropathy. Further research is still needed on many aspects of management
1. The patient, K. Ganga, was admitted to the psychiatry ward for bipolar disorder symptoms including excessive talking, reduced sleep, and indecent behavior observed for 2 months.
2. She was diagnosed with bipolar disorder based on her history of mood fluctuations and manic episodes over 2 years.
3. Her treatment included mood stabilizers, antipsychotics, benzodiazepines, antidepressants, psychotherapy, ECT, and monitoring to reduce her symptoms and prevent relapse. Her symptoms improved over her 3 week hospital stay before she was discharged.
The document presents a case study and article on organophosphate poisoning, describing examples of organophosphates, the history of their development and use, their mechanism of action in poisoning, clinical features depending on route of exposure, and management including gastric lavage, ventilation, and antidotes like atropine and pralidoxime. It then provides details of a specific case of alleged organophosphate poisoning in a 33-year-old male patient who was treated with atropine, pralidoxime, fluids, antibiotics, and counseling.
This document discusses phosphodiesterases (PDEs) as drug targets. PDEs play a major role in cell signaling by regulating levels of cyclic nucleotides like cAMP and cGMP. PDE5 inhibitors like sildenafil (Viagra), vardenafil (Levitra), and tadalafil (Cialis) are approved for treating erectile dysfunction by inhibiting PDE5. This increases cGMP levels and blood flow to the penis. Side effects include headaches and flushing. Care must be taken with drug interactions and in patients using nitrates. Selective inhibition of different PDEs is an area of research for conditions like asthma, COPD, heart failure and inflammation. Effective assays are needed to
Dextroprorpoxyphene is an opioid analgesic used to treat mild pain, cough, and muscle cramps. It acts as an agonist at mu-opioid receptors in the brain and gastrointestinal tract, reducing the perception of pain. However, it can cause dependency among recreational users and has a narrow therapeutic index. A clinical study of 60 patients compared the effects of dextroprorpoxyphene to traditional non-opioid drugs for various conditions like pain, depression, and bronchitis. The study aimed to evaluate dextroprorpoxyphene's adverse effects and judicious use.
Dextropropoxyphene is an opioid analgesic used to treat mild to moderate pain. It acts on opioid receptors in the brain and spinal cord to reduce pain perception and increase tolerance. While it can be effective for its approved uses, it also carries risks of dependency and cardiac side effects when taken in high doses or combined with other central nervous system depressants like alcohol. A clinical study was conducted of 60 patients taking dextropropoxyphene to treat pain, depression, or other conditions. Most patients reported significant relief of symptoms with no side effects after 3 days of treatment. However, dextropropoxyphene must be prescribed judiciously due to its risks and potential for abuse.
study of chf (congestive heart failure) made easy with the help of resent cas...AkshayDeshmukh780714
A 60-year old female patient presented with pedal edema, facial puffiness, shortness of breath, decreased urine output, and generalized swelling. Diagnostic tests revealed right pleural effusion, AV valve sclerosis, mild mitral regurgitation, mild tricuspid regurgitation, moderate pulmonary artery hypertension, and grade II diastolic dysfunction, confirming the diagnosis of congestive heart failure. She was prescribed furosemide, metoprolol, ramipril, esomeprazole, and pantoprazole for treatment and warned about potential drug interactions between the medications. She was counseled on medication adherence, lifestyle modifications including smoking cessation, weight loss, low salt diet,
PHARM-D INTERNSHIP ANNUAL REPORT PRESENTATION UNDER THE GUIDENCE OF DR.R.GO...DR. METI.BHARATH KUMAR
PHARM-D final Internship Report Presentation Under the Guidance of DR.R.Goutham Chakra
If Anyone need this they can contact me via
dr.m.bharathkumar@gmail.com
This document discusses drug interactions, providing examples of potential interactions between antiretroviral drugs and other medications. It defines a drug interaction as when one drug affects another, and describes types of interactions including pharmacokinetic and pharmacodynamic. The document examines case studies of patients taking multiple drugs and identifies possible interaction issues, such as between ketoconazole and an antiretroviral regimen. It emphasizes the importance of considering interactions when starting or changing medications.
Treatment of tuberculosis aims to interrupt transmission and cure patients while preventing drug resistance. First-line drugs include isoniazid, rifampin, pyrazinamide, and ethambutol. Standard treatment involves 6 months of these drugs in two phases. Second-line drugs are used when resistance develops. Treatment is monitored for efficacy and toxicity. Directly observed therapy and prevention measures like the BCG vaccine and contact tracing help control tuberculosis.
Dopamine agonists in advanced Parkinson’s disease.pptxPramod Krishnan
This document summarizes information about dopamine receptor agonists for the treatment of advanced Parkinson's disease. It discusses various dopamine agonists including pramipexole, ropinirole, rotigotine, cabergoline, pergolide, and apomorphine. It reviews their dosages, adverse effects, role in reducing motor fluctuations, and evidence from clinical studies showing benefits of extended release preparations in improving motor symptoms and reducing off time in advanced Parkinson's disease. It highlights the advantages of continuous dopamine replacement therapy for providing more consistent dopamine levels.
Proposing a new indication for Sporanox TM - in the treatment of cancer.
Proposing a new indication for Sporanox TM - in the treatment of cancer.
Proposing a new indication for Sporanox TM - in the treatment of cancer.
Cr 013 presentation sporanox® by carolina hung hoCarolina Hung Ho
I created these slides for the course of CR 013 Pharmacology and Clinical Safety Assessments at AAPS. This purpose of this presentation is to choose an approved medication on the market and propose a new indication in another therapeutic area. I chose Sporanox from Janssen Pharmaceutica and proposed it for the treatment of cancer. Please, enjoy the slides.
This case presentation summarizes the hospital admission of a 35-year-old male diagnosed with Grade II alcoholic liver disease and hepatic encephalopathy. He presented with fever, swelling of the feet and knees, loss of appetite, and sleep issues. His medical history revealed chronic alcohol use and tobacco chewing. On examination, he exhibited pallor, edema, and jaundice. Laboratory tests showed elevated liver enzymes. He was diagnosed with Grade II alcoholic liver disease and hepatic encephalopathy based on his symptoms, risk factors, and diagnostic tests. He was treated medically and counseled on lifestyle modifications and medication adherence.
Clinical trials are research studies that test new treatments for cancer. Every cancer treatment available today was tested in clinical trials first. There are four phases of clinical trials. Phase I trials test safety with a small group. Phase II trials provide initial evidence of effectiveness and further test safety. Phase III trials involve large groups of people to confirm effectiveness, monitor side effects, and compare to standard treatments. Phase IV trials collect longer term safety and effectiveness data after approval.
This document provides an example of performing an ABC analysis on a list of 10 drugs in an inventory. It lists the drugs, their unit costs, total units, and cumulative costs. Based on the cumulative costs, it categorizes the drugs into classes A, B, and C, with class A contributing the most to total costs. The analysis found that 0% of drugs fell into class A, 30% into class B, and 70% into class C.
Clinical trials involve 5 phases (0-4) to study a drug's safety and efficacy in humans. Phase 0 trials use very low doses to determine pharmacokinetics. Phase 1 trials use small groups to determine safety and side effects. Phase 2 trials administer the drug to patients with the target disease to identify effective and safe doses. Phase 3 trials further evaluate safety and efficacy in large patient groups. Phase 4 trials monitor long-term safety and effectiveness after marketing approval and may explore other uses. Successful completion of all phases allows submission of a New Drug Application to regulatory authorities for marketing approval.
This document defines and classifies various sources of drug information. It discusses primary sources like journals and reports that contain original research. Secondary sources analyze and interpret primary sources, including review journals and databases. Tertiary sources combine and summarize primary and secondary sources, such as textbooks and encyclopedias. The document provides examples of specific drug information resources and recommends primary and secondary sources to consult for different types of drug-related questions.
This document discusses the different phases of clinical trials. It explains that clinical trials are conducted in five phases: Phase 0, Phase I, Phase II, Phase III, and Phase IV. Phase 0 involves microdosing to assess pharmacokinetic and pharmacodynamic properties. Phase I studies safety in healthy volunteers. Phase II explores efficacy in patients and determines dosing. Phase III further tests efficacy and safety in larger patient groups. Phase IV occurs after approval to collect additional safety and efficacy data. Together, these phases provide data on new drugs to determine their safety and effectiveness for regulatory approval and marketing.
The document discusses the development of a formulary for a 300 bed teaching hospital. It defines a hospital formulary as a compilation of pharmaceutical agents and dosages selected by the medical staff to be most useful for patient care. It describes the types of formularies as open, closed, or incentive-based. It outlines the steps to prepare a formulary including identifying common diseases, treatments, capabilities, drafting the list, and preparing drug monographs. It also discusses managing the formulary through additions or deletions and periodic reviews. Examples of established formularies are provided and the pharmacist's key role in the development and maintenance of the formulary is highlighted.
The document discusses ABC analysis, an inventory categorization method that divides items into categories A, B, and C based on their annual consumption value. Category A items have the highest value and make up 10-20% of inventory items but 70-80% of total value. Category C items have the lowest value and make up 50% of inventory items but 5% of total value. The document then performs ABC analysis on 10 drugs, finding that 30% of drugs fall into Category B and 70% into Category C, with no drugs in Category A.
The document discusses the development of a hospital formulary for a 300 bed teaching hospital. It defines a hospital formulary and describes the hospital formulary system. There are three main types of formularies: open, closed/restricted, and incentive based. The document outlines the steps to prepare a hospital formulary, including identifying common diseases, creating a draft list, getting department feedback, and preparing drug monographs. It also covers managing the formulary list by adding and deleting drugs based on efficacy, safety, and cost. The roles of the pharmacy department in developing and maintaining the formulary are also summarized.
This document provides information on ABC analysis, a technique for inventory management. It categorizes inventory items into three classes - A, B, and C - based on their value and consumption. Class A items, which are 10% of the inventory but account for 75% of total value, receive the most management attention. Class C items receive the least attention. The document demonstrates performing ABC analysis on a sample pharmacy inventory, categorizing items and discussing applications of the analysis technique.
This document outlines the role and operations of a Pharmacy and Therapeutics Committee in a hospital. The committee is responsible for advising on therapeutic drug use, educating medical staff, and monitoring drug safety and adverse reactions. It is composed of physicians, pharmacists, nurses, and administrators. The committee meets regularly to review formularies, new drugs, adverse reactions, and subcommittee reports. It aims to ensure drug safety through policies like automatic stop orders, emergency drug lists, defect reporting, and drug utilization reviews.
The document discusses the different phases of clinical trials, including:
- Phase I trials test safety on volunteers
- Phase II trials evaluate efficacy on patient populations
- Phase III trials further assess efficacy on larger patient groups to demonstrate safety and effectiveness
It also covers key aspects of clinical trials such as trial teams, the assessment process after a trial is complete, and advantages like providing strong evidence to support policies and minimize bias.
This document provides an overview of the various phases of clinical trials. It discusses phase 0 microdosing trials, phase I safety trials in small patient groups, phase II efficacy trials in larger patient groups, phase III expanded trials to confirm efficacy and safety, and phase IV post-marketing trials. The goal of clinical trials is to systematically study new drugs in human subjects to determine their safety and efficacy.
The document discusses the role and composition of a pharmacy and therapeutics committee in a hospital. The committee is responsible for advising on therapeutic drug use, educating medical staff, and monitoring drug safety and adverse reactions. It is composed of physicians, pharmacists, nurses, and administrators. The committee establishes drug formularies, reviews new drugs, monitors adverse reactions, and ensures emergency drug supplies are available. It aims to promote safe and effective drug use in the hospital.
The document discusses the development of a hospital formulary for a 300 bed teaching hospital. It defines a hospital formulary as a compilation of drugs, dosages, and forms approved by the medical staff. It describes the hospital formulary system and the steps to prepare the formulary including identifying common diseases, treatments, the hospital's capabilities, and obtaining feedback. It also discusses types of formularies, managing the formulary list, maintaining the formulary, examples of other formularies, and the pharmacist's role in the process.
This document discusses various sources of drug information and a systematic approach for providing unbiased drug information. It describes primary, secondary, and tertiary resources. Primary resources include clinical trials and journal articles. Secondary resources are indexing and abstracting services like MEDLINE. Tertiary resources include textbooks, formularies, and drug compendia that summarize and synthesize information from multiple sources. The document emphasizes that tertiary resources are usually the best starting point for answering drug information questions.
This document presents an ABC analysis of 10 drugs in a pharmacy inventory. ABC analysis involves ranking inventory items based on their total cost and dividing them into categories. The analysis showed:
- Category A (10% of items, highest cost) included 1 drug, Amikacin injection
- Category B (40% of items, intermediate cost) included 4 drugs
- Category C (50% of items, lowest cost) included the remaining 5 drugs
The ABC analysis allows the pharmacy to prioritize inventory management efforts based on cost.
This document describes an ABC analysis performed on 10 drugs in a pharmacy inventory. ABC analysis involves categorizing inventory items into A, B, and C categories based on their total cost. The analysis found that 0% of drugs fell into the A category, 10% fell into the B category, and 90% fell into the C category. The C category drugs accounted for the majority (90%) of inventory items but a smaller percentage (40.8%) of total costs. This analysis can help optimize inventory management by prioritizing control measures for higher cost items.
The document discusses the development of a hospital formulary for a 300 bed teaching hospital. It defines a hospital formulary and its objectives which include setting standards for best practice, promoting evidence-based prescribing, and ensuring rational drug therapy and cost control. It describes different types of formularies and the members involved in formulary preparation. It provides guidelines on medicine selection criteria, maintaining and improving adherence to the formulary. The role of pharmacists in the formulary process is also outlined. In conclusion, a well-developed formulary can help set standards for best practice, promote high quality evidence-based prescribing and improve patient outcomes through rational drug therapy.
This document discusses sources of drug information. It defines drug information as the discovery, use, and management of information related to medications, including identification, cost, pharmacokinetics, dosage, and adverse effects. The document classifies sources of drug information as primary, secondary, or tertiary. Primary sources are original materials like journal articles, conference papers, and patents. Secondary sources include review articles and indexes that analyze primary sources. Tertiary sources compile and digest information from primary and secondary sources that has become widely accepted, such as textbooks and databases.
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotesPsychoTech Services
A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
Cell Therapy Expansion and Challenges in Autoimmune DiseaseHealth Advances
There is increasing confidence that cell therapies will soon play a role in the treatment of autoimmune disorders, but the extent of this impact remains to be seen. Early readouts on autologous CAR-Ts in lupus are encouraging, but manufacturing and cost limitations are likely to restrict access to highly refractory patients. Allogeneic CAR-Ts have the potential to broaden access to earlier lines of treatment due to their inherent cost benefits, however they will need to demonstrate comparable or improved efficacy to established modalities.
In addition to infrastructure and capacity constraints, CAR-Ts face a very different risk-benefit dynamic in autoimmune compared to oncology, highlighting the need for tolerable therapies with low adverse event risk. CAR-NK and Treg-based therapies are also being developed in certain autoimmune disorders and may demonstrate favorable safety profiles. Several novel non-cell therapies such as bispecific antibodies, nanobodies, and RNAi drugs, may also offer future alternative competitive solutions with variable value propositions.
Widespread adoption of cell therapies will not only require strong efficacy and safety data, but also adapted pricing and access strategies. At oncology-based price points, CAR-Ts are unlikely to achieve broad market access in autoimmune disorders, with eligible patient populations that are potentially orders of magnitude greater than the number of currently addressable cancer patients. Developers have made strides towards reducing cell therapy COGS while improving manufacturing efficiency, but payors will inevitably restrict access until more sustainable pricing is achieved.
Despite these headwinds, industry leaders and investors remain confident that cell therapies are poised to address significant unmet need in patients suffering from autoimmune disorders. However, the extent of this impact on the treatment landscape remains to be seen, as the industry rapidly approaches an inflection point.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
Tests for analysis of different pharmaceutical.pptx
D.SRUTHI
1. VIGNAN PHARMACY COLLEGE
(APPROVED BY AICTE & PCI AFFILIATED TO JNTU KAKINADA)
VADLAMUDI, GUNTUR DIST, ANDHRA PRADESH, INDIA, PIN: 522 213
2. S. No Drugs ROA Dose Frequency
1 I. Magnex forte IV 1.5gm BID
2 I. Pantoprazole IV 40mg OD
3 I. Citicoline IV 500mg BID
4 T. Ecospirin PO 150mg OD
5 T. Clopidogrel PO 75mg OD
6 T. Atorvastatin PO 40mg Hs
7 Syr. Cremaffin PO 15ml Hs
8 I. Optineuron IV 1amp OD
9 T. Rantac PO 150mg BID
CASE 1:
A 57years old male who is normotensive, non-diabetic presented to hospital with right side dribbling of saliva with slurred
speech and generalized weakness since, seizure like activity.H/O: old CVA with right hemiparesis on medication since 1 year.
Diagnosis: Acute Ischemic Stroke
The medications prescribed are:
3. DRUG INTERACTIONS:
TYPE: Drug- Drug interaction
Finding: Precipitant drug: Clopidogrel
Object drug: Aspirin
Mechanism of Interaction: Pharmacodynamic (synergism)
Assessment: Clopidogrel has been shown to potentiate the inhibition of platelet aggregation due to
aspirin.(These two medications are routinely used together for their additive antiplatelet, antistroke
effect).
Management: Caution is recommended, in patients at risk of bleeding. Patients should be advised to
promptly report any signs of bleeding to their physician. Patients should also be counseled to avoid any
other over-the-counter salicylate products.
4. CASE 2:
A 73years old K/C/O hypertension, parkinson disease, ischemic heart disease, chronic kidney disease, seizures
came with complaints of loose stools of 3 episodes along with fatigue, weakness, dehydration.
Diagnosis: Acute gastroenteritis, K/C/O parkinson’s disease, seizures disorder, ischemic heart disease, hypertension,
chronic kidney disease.
The medications prescribed are:
TYPE: Drug-Drug interaction
Finding: Precipitant drug: Atorvastatin
Object drug: Clopidogrel
Mechanism of Interaction: Pharmacokinetic
Assessment: The concomittant administration of atorvastatin may reduce the metabolic activation of the prodrug
clopidogrel and its antiplatelet effects
Management: Monitoring for altered efficacy of clopidogrel may be advisable if atorvastatin is coadministered
with clopidogrel.
5. S. No Drugs ROA DOSE Frequency
1 T. Ecosprin AV PO 150/20mg OD
2 T. Urimax-D PO 0.4/0.5mg OD
3 T. Ropark PO 0.5mg BID
4 T. Homai-LS PO 1tab OD
5 T. Frisium PO 10mg BID
6 T. Sodamint PO 500mg BID
7 T. Ketoadd PO 1tab OD
8 Cap. Cintodac PO 40/3mg OD
9 T. Syndopa plus PO 100/25mg QID
10 T. Hyponat-O PO 15mg OD
11 Cap. Bio-D3 PO 1tab OD
12 Cap. Providac PO 1cap BID
13 Inj. Ofloxacin IV BID
14 T. Levetiracetam PO 500mg BID
15 T. Eptoin PO 100mg
16 Inj. Pantoprazole IV 40mg OD
17 Inj. Metrogyl IV 500mg TID
18 Syr. Sucralfate PO 2tsp BID
6. DRUG INTERACTIONS:
TYPE: Drug-Drug interaction
Finding: Precipitant drug: Phenytoin
Object drug: Tolvaptan
Mechanism of Interaction: Pharmacokinetic
Assessment: Coadministration with potent inducers of CYP450 3A4 may significantly decrease the plasma concentrations
of tolvaptan.
Management: Concomitant use of tolvaptan with potent CYP450 3A4 inducers should generally be avoided. If
coadministration is necessary, a dosage increase of tolvaptan may be required.
TYPE: Drug- Drug interaction
Finding: Precipitant drug: Benzodiazepines
Object drug: Levodopa
Assessment: Benzodiazepines may decrease the therapeutic effects of levodopa in patients with Parkinson's
disease.
Managaement: Patients receiving this combination should be monitored for altered clinical response. The
benzodiazepine should be discontinued if an interaction is suspected.
7. TYPE:
Therapeutic duplication
The recommended maximum number of medicines in the 'Central Nervous System (CNS) Drugs'
category to be taken concurrently is usually three. But the list includes five medicines belonging to the
'Central Nervous System (CNS) Drugs' category:
Levetiracetam
Ropinirole
Clobazam
carbidopa/levodopa
phenytoin
Note: The benefits of taking this combination of medicines may outweigh any risks associated with
therapeutic duplication.
8. S.No Drugs ROA Dose Frequency
1 Inj. olanzapine IV OD
2 T. Trihexyphenidyl PO 2mg OD
3 Inj. Pantoprazole IV 40mg OD
4 T. Eritel PO 40mg OD
5 T. Ecosprin PO 75mg OD
6 T. Thyronorm PO 25mcg OD
CASE 3:
A 72year old male came with complaints of irrelevant talk, talking to self with abnormal behaviour showing
excess anger with picking clothes and disturbed sleep since 2 days, droswy and unable to from half day.
Diagnosis: Acute psychotic episode with hypertension and hypothyroidism.
The medications prescribed are
9. DRUG INTERACTIONS:
TYPE: Drug- Food interaction
Finding: Precipitant: Alcohol
Object drug: Olanzapine
Mechanism of Interaction: Pharmacokinetic
Assessment: Coadministration with potent inducers of CYP450 3A4 may significantly decrease the plasma
concentrations of tolvaptan.
Management: Patients receiving CNS- active agents should be warned of this interaction and advised to limit or
avoid the consumption of alcohol.
10. TYPE: Drug-Drug interaction
Finding: Precipitant: Certain foods
Objective drug: Levothyroxine
Mechanism of Interaction: Pharmacokinetic
Assessment: Consumption of certain foods as well as timing of meals relative to dosing may affect the
may affect the T4 thyroid hormone.
Management: Preparations containing T4 thyroid hormone should be administered on a consistent
schedule with regard to time of the day and relation to meals so as to avoid large fluctuations in serum
levels. Foods that mat may affect the absorption of T4 should be avoided within several hours of dosing
if possible.