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Map Adverse Drug Events (ADEs) mentioned in text data to their most relevant Preferred MeDDRA terms.
After a second dose of metoclopramide, these symptoms recurred and were associated with confusion, agitation, fever, diaphoresis, tachypnea, tachycardia, and hypertension.
Agitation
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CONCLUSIONS: Clinicians should be aware of a risk of serotonin syndrome with serious extrapyramidal reactions in patients receiving sertraline or venlafaxine when metoclopramide is coadministered even in a single, conventional dose.
Extrapyramidal disorder
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OBJECTIVE: To report 2 cases of serotonin syndrome with serious extrapyramidal movement disorders occurring when metoclopramide was coadministered with sertraline or venlafaxine.
Extrapyramidal disorder
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Serotonin syndrome caused by selective serotonin reuptake-inhibitors-metoclopramide interaction.
Serotonin syndrome
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She was administered metoclopramide because of nausea and, within 2 hours, developed agitation, dysarthria, diaphoresis, and a movement disorder.
Agitation
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She was admitted following a fall and, after being given metoclopramide, developed movement disorder and a period of unresponsiveness.
Movement disorder
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A patient suffering from a rare enzyme deficiency developed a malignant neuroleptic syndrome after having been treated with one single dose of haloperidol.
Neuroleptic malignant syndrome
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BACKGROUND: reports on delated cutaneous reactions to captopril have been seldom reported.
Type IV Hypersensitivity reaction
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Captopril is an angiotensin-converting enzyme (ACE) inhibitor and their cutaneous side-effects are documented, but little has been published concerning the usefulness of patch test when they occur.
Severe cutaneous adverse reaction
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Dermatitis to captopril.
Dermatitis
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We presented the case of a patient who developed a cutaneous reaction induced by captopril with positive patch test.
Severe cutaneous adverse reaction
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A 62-year-old Caucasian man with atrial fibrillation who was taking warfarin reported an episode of hematochezia; his international normalized ratio (INR) was 1.74.
Haematochezia
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Warfarin-associated bleeding complication saved life.
Haemorrhage
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Warfarin-associated bleeding generally is considered deleterious; however, in our patient it unmasked an early stage of colon cancer and thus may have saved the patient's life.
Haemorrhage
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A case of polymyositis with dilated cardiomyopathy associated with interferon alpha treatment for hepatitis B.
Dilated Cardiomyopathy
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In this case, interferon alpha induced polymyositis and cardiomyopathy is diagnosed in a 33-yr-old male patient with history of chronic hepatitis B.
CardioMyopathy
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Polymyositis is a rare complication of interferon alpha treatment as a result of immune-modulating role of the drug itself.
PolyMyositis
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To treat hepatitis B, interferon alpha was administered until the proximal muscle weakness developed.
Muscular weakness
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Aggressive endometrial carcinoma in a breast cancer patient treated with tamoxifen with normal transvaginal ultrasonography.
Endometrial cancer
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Since tamoxifen therapy can induce endometrial disorders, surveillance schemes of women taking tamoxifen have been recommended.
Endometrial cancer
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We described a very atypical case of a high stage, high grade endometrial cancer associated with tamoxifen in a 64-year-old woman with a past history of breast cancer.
Endometrial cancer
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Beginning ductopenia was present in two, suggesting that itraconazole might be responsible for the occurrence of prolonged drug-induced cholangiopathy.
Biliary tract disorder
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CONCLUSIONS: Itraconazole-induced liver injury presents with a cholestatic pattern of injury with damage to the interlobular bile ducts, possibly leading to ductopenia.
Cholestasis
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Hepatotoxicity related to itraconazole: report of three cases.
Hepatotoxicity
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METHODS: Three patients with apparent itraconazole-induced liver injury were studied.
Liver injury
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The occurrence of acute hepatitis is best known for ketoconazole.
Hepatitis
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We report on three patients who developed acute liver damage during therapy with itraconazole, and in whom liver biopsy specimens were obtained.
Hepatocellular injury neonatal
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We suggest that itraconazole should be added to the list of drugs that may be responsible for a drug-induced vanishing bile duct syndrome.
Vanishing bile duct syndrome
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With itraconazole, hepatotoxic reactions have only very rarely been reported, and histologic data are lacking.
Hepatitis toxic
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Thrombotic stroke associated with the use of porcine factor VIII in a patient with acquired haemophilia.
Thrombotic Cerebrovascular accident
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We have recently encountered a patient with acquired haemophilia who developed a thrombotic left middle cerebral artery distribution stroke while being treated with pFVIII.
Thrombotic Cerebrovascular accident
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We speculate that platelet activation induced by pFVIII may have contributed to thrombosis and suggest that pFVIII be used with caution in elderly patients with pre-existing cardiovascular risk factors.
Thrombosis
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Cutaneous sarcoidosis during interferon alfa and ribavirin treatment of hepatitis C virus infection: two cases.
Cutaneous Sarcoidosis
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There have been more than 20 observations of the appearance or aggravation of this granulomatosis with interferon alfa and more recently with the combination of interferon alfa plus ribavirin.
Chronic granulomatous disease
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We report two new cases of sarcoidosis in two patients with hepatitis C virus infection treated with interferon alfa and ribavirin.
Sarcoidosis
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CONCLUSIONS: Although mirtazapine offers clinicians a combination of strong efficacy and good safety, we suggest bearing SS in mind when prescribing this drug, especially in frail, elderly patients with underlying chronic conditions.
Systemic sclerosis pulmonary
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DISCUSSION: A review of the cases of SS with implication of mirtazapine as the cause was performed.
Systemic sclerosis pulmonary
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OBJECTIVE: To document a case of serotonin syndrome (SS) associated with mirtazapine monotherapy, review the previously reported cases of SS associated with this tetracyclic antidepressant, and discuss the possible pathogenic mechanisms leading to this serious adverse drug reaction.
Serotonin syndrome
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Severe serotonin syndrome induced by mirtazapine monotherapy.
Serotonin syndrome
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Pulmonary toxicity secondary to procarbazine.
Pulmonary toxicity
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A 64-year-old man presented with proteinuria during postoperative interferon (IFN)-beta therapy against malignant melanoma.
Proteinuria
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Minimal change nephrotic syndrome developing during postoperative interferon-beta therapy for malignant melanoma.
Nephrotic syndrome
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To our knowledge this is the first report that demonstrates histological abnormalities of the glomerulus associated with postoperative IFN-beta therapy for the malignant melanoma.
Glomerular vascular disorder
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CONCLUSIONS: Clinicians should be aware of the possible association of thrombocytopenia with lansoprazole and discontinue the drug if thrombocytopenia becomes apparent.
Thrombocytopenia
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DISCUSSION: After exclusion of other causes, the onset of thrombocytopenia after administration of lansoprazole, the resolution of the adverse reaction after discontinuation of the drug, and the fact that no other medicines were introduced during this time frame lead us to believe that this was most likely an idiosyncratic thrombocytopenic response to lansoprazole.
Thrombocytopenia
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He was started on oral lansoprazole 60 mg twice daily and, on hospital day 2, his platelet count decreased to 102 x 10(3)/mm(3); on hospital day 3, the platelet count was 36 x 10(3)/mm(3).
Platelet count decreased
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Lansoprazole-induced thrombocytopenia.
Thrombocytopenia
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OBJECTIVE: To describe a case of thrombocytopenia associated with the administration of lansoprazole.
Thrombocytopenia
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To date, this is the first reported case of what appears to be isolated thrombocytopenia associated with lansoprazole.
Thrombocytopenia
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Life-threatening anaphylactoid reaction to amifostine used with concurrent chemoradiotherapy for nasopharyngeal cancer in a patient with dermatomyositis: a case report with literature review.
Anaphylactoid reaction
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The most common side effects associated with amifostine are nausea, vomiting, hypotension, hypocalcemia and allergic reactions.
Hypersensitivity
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The patient suffered a life-threatening anaphylactoid reaction to amifostine.
Anaphylactoid reaction
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Agranulocytosis during clozapine therapy.
Agranulocytosis
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Granulocytopenia and agranulocytosis are considered among the most dangerous adverse effects of clozapine.
Agranulocytosis
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The female patient received clozapine in a daily dose of 400 mg, which induced agranulocytosis after 2 months.
Agranulocytosis
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The male patient was treated with 225-mg/day clozapine and the time to the diagnosis of agranulocytosis was 6 weeks.
Agranulocytosis
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A 53-year-old man developed NMS without rigidity while taking olanzapine.
Neuroleptic malignant syndrome
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Atypical neuroleptic malignant syndrome associated with olanzapine.
Neuroleptic malignant syndrome
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CASE SUMMARY: We report the case of a 31-year-old patient hospitalized due to behavioral alterations and treated with oral zuclopenthixol, an antipsychotic from the thioxanthene family, who developed an acute, painful erection.
Painful erection
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CONCLUSIONS: Priapism is an uncommon but potentially serious adverse effect of zuclopenthixol that practitioners, as with many other antipsychotics, should be aware of.
Priapism
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DISCUSSION: The occurrence of priapism in our patient was related to zuclopenthixol.
Priapism
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OBJECTIVE: To present a single case of zuclopenthixol-induced priapism and a literature review.
Priapism
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Priapism associated with zuclopenthixol.
Priapism
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The capacity of zuclopenthixol to induce priapism is thought to be due to its antagonist activity on alpha-adrenergic receptors.
Priapism
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After identification of the index patient, additional inquiry revealed that the patient's mother was hospitalized previously for overwhelming sepsis associated with metamizole use.
Sepsis
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Metamizole, a nonsteroidal antiinflammatory agent, is prohibited in the United States because of the risk of agranulocytosis but is widely used in Mexico and other countries.
Agranulocytosis
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Erythropoietin is beneficial in mitomycin-induced hemolytic-uremic syndrome.
Haemolytic uraemic syndrome
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We describe a patient who developed HUS after treatment with mitomycin C (total dose 144 mg/m2) due to a carcinoma of the ascending colon.
Haemolytic uraemic syndrome
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Levofloxacin-induced toxic epidermal necrolysis in an elderly patient.
Toxic epidermal necrolysis
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To our knowledge, this case is the first published report of levofloxacin-induced TEN.
Toxic epidermal necrolysis
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A 31-year-old female developed multiple episodes of grand mal seizures after combination chemotherapy with cisplatin, vinblastine and bleomycin for germ cell ovarian cancer stage Ic.
Generalised tonic-clonic seizure
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Posterior leukoencephalopathy following cisplatin, bleomycin and vinblastine therapy for germ cell tumor of the ovary.
Posterior reversible encephalopathy syndrome
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After 5 days of treatment with IL-2, the patient developed a hemorrhagic lesion that progressed to toxic epidermal necrolysis, as well as grade 4 pancytopenia.
Hemorrhagic lesion
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OBJECTIVE: To report a case of cutaneous and hematologic toxicity in a patient treated with IL-2.
cutaneous and hematologic toxicity
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Toxic epidermal necrolysis associated with interleukin-2.
Toxic epidermal necrolysis
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A case of anaphylactoid reaction due solely to the use of Gelofusine in a patient with non-haemorrhagic hypovolaemia is presented, with a discussion on the management and the use of allergy identification jewellery.
Anaphylactoid reaction
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Gelofusine allergy--the need for identification jewellery.
Hypersensitivity
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The authors describe valproate-induced hyperammonemia and mental status changes in an 88-year-old man, the first known reported case in an elderly patient.
Hyperammonaemia
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Valproate-induced hyperammonemia as a cause of altered mental status.
Altered state of consciousness
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Leiomyosarcoma in urinary bladder after cyclophosphamide therapy for retinoblastoma and review of bladder sarcomas.
LeiomyosarComa
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The epivodes of NMS occured under treatment with clozapine, risperidone, and amisulpride.
Neuroleptic malignant syndrome
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A 73-year-old woman presented with fever and cough 2 weeks after completing the third cycle of fludarabine for chronic lymphocytic leukemia (CLL).
Cough
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Fludarabine induced lung toxicity must be considered in all patients who develop unexplained lung disease while receiving fludarabine.
Lung disorder
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Multiple pulmonary nodules: an unusual presentation of fludarabine pulmonary toxicity: case report and review of literature.
Milker's nodules
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This case extends the spectrum of fludarabine pulmonary toxicity to include pulmonary nodules.
Milker's nodules
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To our knowledge, four cases of interstitial pneumonitis associated with fludarabine have been reported in medical literature.
Interstitial lung disease
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Epoprostenol may be associated rarely with severe erythroderma.
Dermatitis exfoliative generalised
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Severe erythroderma as a complication of continuous epoprostenol therapy.
Dermatitis exfoliative generalised
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We report a case of a patient with pulmonary hypertension and undifferentiated connective tissue disease who, after 2 months of treatment with epoprostenol, presented with rapidly progressive erythema, scaling, nausea and vomiting, and fever.
Pyrexia
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A 50-year-old diabetic and hypertensive male patient is reported who had ticlopidine-induced marrow aplasia partially responsive to colony-stimulating factors and corticosteroids, but experienced complete recovery with cyclosporine.
Febrile bone marrow aplasia
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There is no consensus on the treatment of ticlopidine-induced marrow aplasia.
Febrile bone marrow aplasia
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Ticlopidine-induced marrow aplasia treated with cyclosporine.
Febrile bone marrow aplasia
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A 53-year-old man developed lower leg edema 4 weeks after rosiglitazone was increased from 4 mg once/day to 4 mg twice/day.
OOedema peripheral
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A 75-year-old man developed bilateral lower leg edema 6 months after switching from troglitazone to pioglitazone.
OOedema peripheral
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A 77-year-old man developed ankle, hand, and facial swelling 2 weeks after starting rosiglitazone.
Peripheral swelling
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Two cases of polymorphic ventricular tachycardia induced by the administration of verapamil against paroxysmal supraventricular tachycardia.
Ventricular tachycardia
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Verapamil is widely used for the termination of paroxysmal supraventricular tachycardia (PSVT) with little proarrhythmic effect.
Arrhythmia
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We describe two cases of PSVT that changed to non-sustained polymorphic ventricular tachycardia after administration of verapamil.
Ventricular tachycardia
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Epsilon-aminocaproic acid and renal complications: case report and review of the literature.
Mydriasis
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We present a neonate with a seizure disorder who acutely developed pupillary mydriasis secondary to lidocaine overdose.
Mydriasis