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There have been reported instances of prolonged jaundice, extrapyramidal signs, hyperreflexia or hyporeflexia in newborn infants whose mothers received phenothiazines.

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Prochlorperazine may impair prochlorperazine sleeping tablets and/or physical abilities, especially during the first few days of therapy. Therefore, caution patients about activities requiring alertness e.Symptoms may include mask-like faces, drooling, tremors, pillrolling motion, cogwheel rigidity, and shuffling gait.

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Begin with the lowest recommended dose. Although response prochlorperazine stemetil is seen within a day or two, longer treatment is usually required before maximal improvement is seen.Specifically, the risk of gastrointestinal adverse effects may be increased.

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Reassurance and sedation are important.This medication may interfere with certain laboratory tests including phenylketonuria, certain pregnancy tests possibly causing false test results.

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The presence of phenothiazines may produce false-positive phenylketonuria PKU test results. Given the likelihood that some patients exposed chronically to antipsychotics will develop tardive dyskinesia, it is advised that all patients in whom chronic use is contemplated be given, if possible, full information about this prochlorperazine 5 mg.

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There have been a few observations of fatty changes in the livers of patients who have died while receiving the drug. o causal relationship has been established.Consult your pharmacist prochlorperazine 5 mg local waste disposal company for more details about how to safely discard your product.

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Many drugs can affect prochlorperazine, especially: This list is not complete and many other drugs may affect prochlorperazine. This includes prescription and over-the-counter medicines, vitamins, and herbal products.PO: Immediate-release, 5-10 mg q6-8hr; extended-release, 10 mg q12hr prochlorperazine 5 mg 15 mg every morning Suppository: 25 mg q12hr IM: 5-10 mg q3-4hr; not to exceed 40 mg/day IV: 2.

-10 mg q3-4hr; not to exceed 10 mg/dose or 40 mg/day Prophylaxis IM: 5-10 mg administered 1-2 hours before induction of anesthesia; may prochlorperazine 5 mg repeated once 30 minutes prochlorperazine 5 mg initial dose IV: 5-10 mg administered 15-30 minutes before induction of anesthesia, repeated once before procedure if desired, or 20 mg/L administered 15-30 minutes before induction; not to exceed 30 mg/day 5-10 mg PO q6-8hr; slowly titrate dose q2-3days; not to exceed 150 mg/day 10-20 mg IM q2-4hr to gain control; 3-4 doses rarely neededInsomnia Restlessness immediate restlessness or agitation may be treated with diphenhydramine 25 mg IV push Dizziness Anxiety Euphoria Agitation Depression Weakness Headache Cerebral edema Poikilothermia Orthostatic hypotension after IM injection Tachycardia ECG changes Anorexia Dyspepsia Constipation Diarrhea Ileus Blood dyscrasia Galactorrhea Gynecomastia Ejaculatory disorder Lens opacities with prolonged use Photosensitivity Prochlorperazine 5 mg Akathisia Sedation Anticholinergic effects Weight gain Oligomenorrhea or amenorrhea Erectile dysfunction Extrapyramidal prochlorperazine 5 mg muscle stiffness, dystonia, parkinsonism, tardive dyskinesia Neuroleptic malignant syndrome infrequent but serious Seizure Decreased gag reflex Confusion Hypotension Hypertension Leukopenia Agranulocytosis Cholestatic jaundice Photosensitivity reaction Priapism Hepatotoxicity Patients with dementia-related psychosis who are treated with antipsychotic prochlorperazine 5 mg are at an increased risk of death, as shown in short-term controlled trials; the deaths appeared to be either cardiovascular eg, heart failure, sudden death or infectious eg, pneumonia in nature This drug is not approved for treatment of prochlorperazine 5 mg with dementia-related psychosisDocumented hypersensitivity to phenothiazines Coma, severe CNS depression, concurrent use of large amounts of CNS depressants, poorly controlled seizure disorder, subcortical brain damage Postoperative management of nausea/vomiting following pediatric surgery Children 9 kg Avoid using in children with suspected Reye syndrome Use caution in evere hypertension, severe cardiovascular disease Use with caution in glaucoma, prostatic hypertrophy, stenosing peptic ulcer disease, history of neuroleptic malignant syndrome, Parkinson disease, hypocalcemia, renal/hepatic impairment, history of severe reactions to insulin or electroconvulsive therapy, history of seizures, asthma, respiratory tract infections, cardiovascular disease, myelosuppression Blood dyscrasias including neutropenia, agranulocytosis, and leukopenia reported with use; discontinue therapy at first sign of blood dyscrasias Risk of extrapyramidal symptoms, neuroleptic malignant syndrome, hypotension may be particularly severe in patients with pheochromocytoma or mitral insufficiency Esophageal dysmotility/aspiration may occur; use with caution in patients at risk of pneumonia Depresses hypothalamic thermoregulatory prochlorperazine 5 mg exposure to extreme temperatures may cause hypo- or hyperthermia May alter cardiac conduction; life-threatening arrhythmias reported with therapeutic doses May cause anticholinergic effects constipation, xerostomia, urinary retention, blurred vision use caution in patients with decreased gastrointestinal motility, paralytic ileus, urinary retention, BPH, xerostomia, visual problems May cause pigmentary retinopathy and lenticular and prochlorperazine 5 mg deposits, especially in prolonged therapy May cause sedation and impair ability to perform tasks which require mental alertness, including operating heavy machinery Use associated with increased prolactin levels In case of prochlorperazine 5 mg hypotension, use norepinephrine or phenylepinephrine; do not use epinephrine or dopamine Do not crush extended-release product Avoid SC administration may cause irritation Antiemetic effect may obscure toxicity of chemotherapeutic drugs Use may be associated with neuroleptic malignant syndrome; monitor muscle rigidity, mental status changes, fever, autonomic instability May need anticholinergic antiparkinsonian agent to counter extrapyramidal symptoms May impair core body temperature regulation FDA warning regarding off-label use for dementia in elderly Pregnancy category: C Lactation: Phenothiazines prochlorperazine 5 mg be excreted in breast milk; do not nurseA: Generally acceptable.

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6 mg of the drug per lb of body weight; give by deep IM injection.Antipsychotic drug treatment itself, however, may suppress prochlorperazine 5 mg partially suppress the signs and symptoms of the syndrome and thereby may possibly mask the underlying disease process.

The effect that symptomatic suppression has upon the long-term course of the syndrome is unknown.

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Dystonic symptoms include: spasm of the neck muscles, prochlorperazine sleeping tablets progressing to tightness of the throat, swallowing difficulty, difficulty breathing, and/or protrusion of the tongue.Should it be necessary to reinstitute treatment, or increase the dosage of the agent, or switch to a different antipsychotic agent, the syndrome may be masked.

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The decision to inform patients and/or their guardians must obviously take into account the clinical circumstances and the competency of the prochlorperazine stemetil to understand the information provided.The need for continued treatment should be reassessed periodically.

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This may lead to a higher chance of infection.Other possible manifestations include convulsions, EKG changes and cardiac arrhythmias, fever, and autonomic reactions such as hypotension, dry mouth and ileus.

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