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Norcuron adverse events reported to FDA.

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Summary

FDA Adverse Reports: 9. View All

Norcuron FDA safety alerts: No

Reported deaths: 4

Reported hospitalizations: 2

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Often additional risks of using a medication, such as Norcuron, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Norcuron users, Learn more about unwanted side effects & find ways to reduce them. Browse Norcuron Adverse Reports reported to FDA and participate in Norcuron discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Norcuron. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Norcuron Adverse Effect Reports (FDA)

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6669811-6 | Breath Holding, Bronchospasm, Increased Bronchial Secretion
on Mar 26, 2010 Female patient from INDIA , 29 years of age, was treated with Norcuron (View Usage). Patient experienced the following unwanted or unexpected effects: breath holding, bronchospasm, increased bronchial secretion. Norcuron dosage: Iv. During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ).

6592992-X | Anaphylactic Shock
Patient was taking Norcuron (View Usage). Patient had the following side effects: anaphylactic shock on Jan 29, 2010 from FRANCE Additional patient health information: Female patient , 83 years of age, . Norcuron dosage: 5 Mg; Once; Iv. During the same period patient was treated with CEFAMANDOLE (CEFAMANDOLE) (750 Mg; Once; Iv) (View Cefamandole (cefamandole) Review and Cefamandole (cefamandole) Label ), ETOMIDATE (24 Mg; Once; Iv) (View Etomidate Review and Etomidate Label ), SUFENTANIL CITRATE (5 Mcg; Once; Iv) (View Sufentanil Citrate Review and Sufentanil Citrate Label ), CORGARD (View Corgard Review and Corgard Label ).

6592879-2 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Lactate Dehydrogenase Increased, Gamma-glutamyltransferase Increased, Liver Injury, Post Procedural Complication
Adverse event was reported on Jan 18, 2010 by a Female patient taking Norcuron (View Usage) (Dosage: ) . Location: AUSTRALIA , 80 years of age, weighting 130.1 lb, After Norcuron was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, liver injury, post procedural complication. During the same period patient was treated with GENTAMICIN SULFATE (View Gentamicin Sulfate Review and Gentamicin Sulfate Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ), FENTANYL 100 (View Fentanyl-100 Review and Fentanyl-100 Label ), METRAMINOL TARTATE (METARAMINOL TARTRATE) (View Metraminol Tartate (metaraminol Tartrate) Review and Metraminol Tartate (metaraminol Tartrate) Label ), ONDANSETRON HYDROCHLORIDE DIHYDRATE (ONDANSETRON HYDROCHLORIDE) (View Ondansetron Hydrochloride Dihydrate (ondansetron Hydrochloride) Review and Ondansetron Hydrochloride Dihydrate (ondansetron Hydrochloride) Label ), VANCOMYCIN HYDROCHLORIDE (View Vancomycin Hydrochloride Review and Vancomycin Hydrochloride Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), AMITRIPTYLINE HYDROCHLORIDE (View Amitriptyline Hydrochloride Review and Amitriptyline Hydrochloride Label ). Patient was hospitalized.

6580246-7 | Anaphylactic Shock, Circulatory Collapse
on Jan 29, 2010 Female patient from FRANCE , 83 years of age, was treated with Norcuron (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock, circulatory collapse. Norcuron dosage: 5 Mg; Once; Iv. During the same period patient was treated with CEFAMANDOLE (CEFAMANDOLE) (750 Mg; Once; Iv) (View Cefamandole (cefamandole) Review and Cefamandole (cefamandole) Label ), ETOMIDATE (24 Mg; Once; Iv) (View Etomidate Review and Etomidate Label ), SUFENTANIL CITRATE (5 Mcg; Once; Iv) (View Sufentanil Citrate Review and Sufentanil Citrate Label ), CORGARD (View Corgard Review and Corgard Label ).


6565872-3 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Lactate Dehydrogenase Increased, Gamma-glutamyltransferase Increased, Liver Injury
on Jan 18, 2010 Female patient from AUSTRALIA , 80 years of age, weighting 130.1 lb, was treated with Norcuron (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, liver injury. Norcuron dosage: . During the same period patient was treated with FENTANYL 100 (View Fentanyl-100 Review and Fentanyl-100 Label ), GENTAMICIN SULFATE (View Gentamicin Sulfate Review and Gentamicin Sulfate Label ), METARAMINOL BITARTRATE (View Metaraminol Bitartrate Review and Metaraminol Bitartrate Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ), ONDANSETRON HCL (View Ondansetron Hcl Review and Ondansetron Hcl Label ), PARACETAMOL /00020001/ (PARACETAMOL /00020001/) (View Paracetamol /00020001/ (paracetamol /00020001/) Review and Paracetamol /00020001/ (paracetamol /00020001/) Label ), VANCOMYCIN HYDROCHLORIDE (View Vancomycin Hydrochloride Review and Vancomycin Hydrochloride Label ), AMITRIPTYLINE HYDROCHLORIDE (View Amitriptyline Hydrochloride Review and Amitriptyline Hydrochloride Label ). Patient was hospitalized.

6552916-8 | Anaphylactic Shock
Patient was taking Norcuron (View Usage). After Norcuron was administered, patient had the following side effects: anaphylactic shock on Jan 19, 2010 from FRANCE Additional patient health information: Female patient , 84 years of age, . Norcuron dosage: Once;iv. During the same period patient was treated with CEFAMNDOLE (CEFAMANDOLE) (Once;iv) (View Cefamndole (cefamandole) Review and Cefamndole (cefamandole) Label ).

6542829-X | Anaphylactic Shock
Adverse event was reported on Jan 05, 2010 by a Female patient taking Norcuron (View Usage) (Dosage: Once; Iv) . Location: FRANCE , 84 years of age, Patient experienced the following unwanted or unexpected effects: anaphylactic shock. During the same period patient was treated with CEFAMANDOLE (CEFAMANDOLE) (Once; Iv) (View Cefamandole (cefamandole) Review and Cefamandole (cefamandole) Label ).

6327728-0 | Fear, Paralysis Flaccid, Respiratory Arrest
on Aug 07, 2009 Male patient from UNITED STATES , child 3 years of age, was treated with Norcuron (View Usage). Patient had the following side effects: fear, paralysis flaccid, respiratory arrest. Norcuron dosage: Once;. During the same period patient was treated with SALINE (View Saline Review and Saline Label ).

5708751-3 | Asthma, Prolonged Expiration
on Apr 02, 2008 Female patient from JAPAN , 49 years of age, was diagnosed with induction of anaesthesia and was treated with Norcuron (View Usage). After Norcuron was administered, patient had the following side effects: asthma (What is asthma?), prolonged expiration. Norcuron dosage: 1.5 Mg/kg Once Intravenous (nos). During the same period patient was treated with MIDAZOLAM HCL (0.1 Mg/kg Once Intravenous (nos)) (View Midazolam Hcl Review and Midazolam Hcl Label ), FENTANYL CITRATE (0.5 Ug/kg Once Intravenous (nos)) (View Fentanyl Citrate Review and Fentanyl Citrate Label ), BETAMETHASONE SODIUM PHOSPHATE (View Betamethasone Sodium Phosphate Review and Betamethasone Sodium Phosphate Label ).


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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Norcuron risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Norcuron quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Norcuron use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Norcuron Reactions
Alanine Aminotransferase Increased
Anaphylactic Shock
Aspartate Aminotransferase Increased
AsthmaWhat is Asthma?
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
Blood Lactate Dehydrogenase Increased
Breath Holding
Bronchospasm
Circulatory Collapse
Fear
Gamma-glutamyltransferase Increased
Increased Bronchial Secretion
Liver Injury
Paralysis Flaccid
Post Procedural Complication
Prolonged Expiration
Respiratory Arrest
Norcuron Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Norcuron adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!