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Summary

FDA Adverse Reports: 31. View All

Tracrium FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 14

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Often additional risks of using a medication, such as Tracrium, 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 Tracrium users, Learn more about unwanted side effects & find ways to reduce them. Browse Tracrium Adverse Reports reported to FDA and participate in Tracrium discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Tracrium. 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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Tracrium Adverse Effect Reports (FDA)

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6525826-X | Anaphylactic Shock, Bradycardia, Bronchospasm, Circulatory Collapse, Hypotension
on Dec 24, 2009 Male patient from FRANCE , 34 years of age, was diagnosed with prophylaxis and was treated with Tracrium (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock, bradycardia, bronchospasm, circulatory collapse, hypotension. Tracrium dosage: . During the same period patient was treated with AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), SUFENTANIL CITRATE (View Sufentanil Citrate Review and Sufentanil Citrate Label ).

6470768-1 | Anaphylactic Shock, Bradycardia, Bronchospasm, Circulatory Collapse, Hypotension
Patient was taking Tracrium (View Usage). Patient had the following side effects: anaphylactic shock, bradycardia, bronchospasm, circulatory collapse, hypotension on Nov 23, 2009 from FRANCE Additional patient health information: Male patient , 34 years of age, was diagnosed with prophylaxis and. Tracrium dosage: . During the same period patient was treated with AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), SUFENTANIL CITRATE (View Sufentanil Citrate Review and Sufentanil Citrate Label ).

6138261-3 | Anaphylactic Shock, Circulatory Collapse, Tachycardia
Adverse event was reported on Mar 20, 2009 by a Female patient taking Tracrium (View Usage) (Dosage: 25mg Single Dose) was diagnosed with plasma expander transfusion, antibiotic prophylaxis and. Location: FRANCE , 78 years of age, After Tracrium was administered, patient had the following side effects: anaphylactic shock, circulatory collapse, tachycardia. During the same period patient was treated with GELOFUSINE (200ml Per Day) (View Gelofusine Review and Gelofusine Label ), CEFAZOLIN (View Cefazolin Review and Cefazolin Label ). Patient was hospitalized.

6080571-2 | Anaphylactic Shock, Hypotension
on Feb 06, 2009 Female patient from FRANCE , 55 years of age, was diagnosed with tumour excision, hypothyroidism and was treated with Tracrium (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock, hypotension. Tracrium dosage: . During the same period patient was treated with BLEU PATENT (View Bleu Patent Review and Bleu Patent Label ), CEFAZOLIN (2g Single Dose) (View Cefazolin Review and Cefazolin Label ), SUFENTA PRESERVATIVE FREE (View Sufenta Preservative Free Review and Sufenta Preservative Free Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), LEVOTHYROX (View Levothyrox Review and Levothyrox Label ).


6048489-9 | Agitation, Anaphylactic Shock, Blood Pressure Immeasurable, Cardiac Arrest, Cardiac Enzymes Increased, Hepatocellular Injury, Hypokalaemia, Inflammation
on Jan 19, 2009 Male patient from FRANCE , 40 years of age, was diagnosed with antibiotic prophylaxis and was treated with Tracrium (View Usage). Patient had the following side effects: agitation, anaphylactic shock, blood pressure immeasurable, cardiac arrest (What is cardiac arrest?), cardiac enzymes increased, hepatocellular injury, hypokalaemia, inflammation. Tracrium dosage: . During the same period patient was treated with DIPRIVAN (150mg Per Day) (View Diprivan Review and Diprivan Label ), SUFENTA PRESERVATIVE FREE (10mcg Per Day) (View Sufenta Preservative Free Review and Sufenta Preservative Free Label ), CEFACIDAL (2g Per Day) (View Cefacidal Review and Cefacidal Label ).

5940327-5 | Anaphylactic Shock, Cardiac Arrest, Erythema, Tachycardia
Patient was taking Tracrium (View Usage). After Tracrium was administered, patient had the following side effects: anaphylactic shock, cardiac arrest (What is cardiac arrest?), erythema, tachycardia on Oct 30, 2008 from FRANCE Additional patient health information: Male patient , 40 years of age, . Tracrium dosage: . During the same period patient was treated with DIPRIVAN (150mg Per Day) (View Diprivan Review and Diprivan Label ), SUFENTA PRESERVATIVE FREE (10mcg Per Day) (View Sufenta Preservative Free Review and Sufenta Preservative Free Label ), CEFACIDAL (2g Per Day) (View Cefacidal Review and Cefacidal Label ). Patient was hospitalized.

5757081-2 | Anaphylactic Shock, Blood Pressure Decreased, Face Oedema, Haemodynamic Instability, Local Swelling, Oedema Peripheral, Rash, Skin Discolouration, Swelling Face
Adverse event was reported on May 23, 2008 by a Male patient taking Tracrium (View Usage) (Dosage: 20mg Per Day) . Location: SWITZERLAND , 13 years of age, weighting 110.2 lb, Patient experienced the following unwanted or unexpected effects: anaphylactic shock, blood pressure decreased, face oedema, haemodynamic instability, local swelling, oedema peripheral, rash (What is rash?), skin discolouration, swelling face. During the same period patient was treated with HETASTARCH + SODIUM CHLORIDE (View Hetastarch + Sodium Chloride Review and Hetastarch + Sodium Chloride Label ), KEFZOL (View Kefzol Review and Kefzol Label ), HEPARIN SODIUM (View Heparin Sodium Review and Heparin Sodium Label ), THIOPENTAL SODIUM (View Thiopental Sodium Review and Thiopental Sodium Label ), FENTANYL 100 (View Fentanyl-100 Review and Fentanyl-100 Label ), ULTIVA (View Ultiva Review and Ultiva Label ), INTUBATION (View Intubation Review and Intubation Label ). Patient was hospitalized.

5597604-X | Bronchospasm, Rash
on Jan 10, 2008 Male patient from FRANCE , 22 years of age, was treated with Tracrium (View Usage). Patient had the following side effects: bronchospasm, rash (What is rash?). Tracrium dosage: 35mg Single Dose. During the same period patient was treated with DIPRIVAN (200mg Single Dose) (View Diprivan Review and Diprivan Label ), SUFENTA (15mcg Single Dose) (View Sufenta Review and Sufenta Label ), CEFAZOLIN (2g Per Day) (View Cefazolin Review and Cefazolin Label ), KETAMINE HCL (10mg Single Dose) (View Ketamine Hcl Review and Ketamine Hcl Label ). Patient was hospitalized.

5532076-2 | Abdominal Pain, Pancreatitis Acute
on Nov 28, 2007 Female patient from FRANCE , 44 years of age, was treated with Tracrium (View Usage). After Tracrium was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), pancreatitis acute. Tracrium dosage: 30mg Single Dose. During the same period patient was treated with VENTOLIN (2unit Single Dose) (View Ventolin Review and Ventolin Label ), VANCOMYCIN (1g Single Dose) (View Vancomycin Review and Vancomycin Label ), DESFLURANE (View Desflurane Review and Desflurane Label ), SUFENTA (30mcg Single Dose) (View Sufenta Review and Sufenta Label ), PROPOFOL (150mg Single Dose) (View Propofol Review and Propofol Label ), SPASMINE (View Spasmine Review and Spasmine Label ). Patient was hospitalized.

5510742-2 | C-reactive Protein Increased, Dermatomyositis, Dyspnoea, Erythema, Leg Amputation, Lung Disorder, Lymphocele, Lymphopenia, Neoplasm
Patient was taking Tracrium (View Usage). Patient experienced the following unwanted or unexpected effects: c-reactive protein increased, dermatomyositis, dyspnoea, erythema, leg amputation, lung disorder, lymphocele, lymphopenia, neoplasm on Oct 30, 2007 from FRANCE Additional patient health information: Male patient , 69 years of age, weighting 158.7 lb, . Tracrium dosage: . During the same period patient was treated with AUGMENTIN (View Augmentin Review and Augmentin Label ), NIMBEX (View Nimbex Review and Nimbex Label ), KETOPROFEN (View Ketoprofen Review and Ketoprofen Label ), CIPROFLOXACIN HCL (View Ciprofloxacin Hcl Review and Ciprofloxacin Hcl Label ), SEVOFLURANE (View Sevoflurane Review and Sevoflurane Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), SUFENTANIL CITRATE (View Sufentanil Citrate Review and Sufentanil Citrate Label ), ETOMIDATE (View Etomidate Review and Etomidate Label ). Patient was hospitalized.

5451417-8 | C-reactive Protein Increased, Dermatomyositis, Dyspnoea, Erythema, Leg Amputation, Lung Disorder, Lymphocele, Lymphopenia, Neoplasm
Adverse event was reported on Sep 03, 2007 by a Male patient taking Tracrium (View Usage) (Dosage: ) was diagnosed with anaesthesia and. Location: FRANCE , 69 years of age, weighting 158.7 lb, Patient had the following side effects: c-reactive protein increased, dermatomyositis, dyspnoea, erythema, leg amputation, lung disorder, lymphocele, lymphopenia, neoplasm. During the same period patient was treated with AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), NIMBEX (View Nimbex Review and Nimbex Label ), PROFENID (View Profenid Review and Profenid Label ), CIFLOX (View Ciflox Review and Ciflox Label ), SEVOFLURANE (View Sevoflurane Review and Sevoflurane Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), SUFENTANIL CITRATE (View Sufentanil Citrate Review and Sufentanil Citrate Label ), ETOMIDATE (View Etomidate Review and Etomidate Label ). Patient was hospitalized.

5423684-8 | Anaphylactic Shock, Histamine Level Increased, Hypotension, Tryptase Increased
on Aug 17, 2007 Female patient from FRANCE , 58 years of age, was treated with Tracrium (View Usage). After Tracrium was administered, patient had the following side effects: anaphylactic shock, histamine level increased, hypotension, tryptase increased. Tracrium dosage: . During the same period patient was treated with HYPNOVEL (View Hypnovel Review and Hypnovel Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), KETAMINE HCL (View Ketamine Hcl Review and Ketamine Hcl Label ), SUFENTANIL CITRATE (View Sufentanil Citrate Review and Sufentanil Citrate Label ), CEFUROXIME (View Cefuroxime Review and Cefuroxime Label ).

5358907-7 | Bronchospasm, Hypotension, Laryngospasm, Rash Erythematous
on Jun 05, 2007 Female patient from FRANCE , 30 years of age, was treated with Tracrium (View Usage). Patient experienced the following unwanted or unexpected effects: bronchospasm, hypotension, laryngospasm, rash erythematous. Tracrium dosage: 25mg Per Day. During the same period patient was treated with AUGMENTIN '125' (1g Per Day) (View Augmentin '125' Review and Augmentin '125' Label ), CLAMOXYL IV (1g Per Day) (View Clamoxyl Iv Review and Clamoxyl Iv Label ), HYPNOVEL (3mg Per Day) (View Hypnovel Review and Hypnovel Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), SUFENTANIL CITRATE (30mcg Per Day) (View Sufentanil Citrate Review and Sufentanil Citrate Label ).

5323823-3 | Blood Creatine Phosphokinase Increased, Muscle Necrosis, Myoglobin Urine Present, Rhabdomyolysis
Patient was taking Tracrium (View Usage). Patient had the following side effects: blood creatine phosphokinase increased, muscle necrosis, myoglobin urine present, rhabdomyolysis on May 03, 2007 from FRANCE Additional patient health information: Male patient , 44 years of age, was diagnosed with asthma (What is asthma?), asthmatic crisis and. Tracrium dosage: . During the same period patient was treated with SALBUTAMOL (View Salbutamol Review and Salbutamol Label ), SOLU MEDROL (View Solu-medrol Review and Solu-medrol Label ), SINGULAIR (View Singulair Review and Singulair Label ), SERETIDE (View Seretide Review and Seretide Label ), DESLORATADINE (View Desloratadine Review and Desloratadine Label ), VENTOLIN (View Ventolin Review and Ventolin Label ). Patient was hospitalized.

5317918-8 | Bronchospasm, Hypotension, Rash Erythematous
Adverse event was reported on Apr 27, 2007 by a Female patient taking Tracrium (View Usage) (Dosage: 25mg Single Dose) . Location: FRANCE , 30 years of age, After Tracrium was administered, patient had the following side effects: bronchospasm, hypotension, rash erythematous. During the same period patient was treated with AUGMENTIN '125' (2g Per Day) (View Augmentin '125' Review and Augmentin '125' Label ), CLAMOXYL IV (View Clamoxyl Iv Review and Clamoxyl Iv Label ), HYPNOVEL (View Hypnovel Review and Hypnovel Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), SUFENTANIL CITRATE (View Sufentanil Citrate Review and Sufentanil Citrate Label ).

5275792-2 | C-reactive Protein Increased, Dermatomyositis, Dyspnoea, Erythema, Leg Amputation, Lung Disorder, Lymphocele, Lymphopenia, Neoplasm
on Mar 13, 2007 Male patient from FRANCE , 69 years of age, weighting 158.7 lb, was treated with Tracrium (View Usage). Patient experienced the following unwanted or unexpected effects: c-reactive protein increased, dermatomyositis, dyspnoea, erythema, leg amputation, lung disorder, lymphocele, lymphopenia, neoplasm. Tracrium dosage: . During the same period patient was treated with AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), NIMBEX (View Nimbex Review and Nimbex Label ), KETOPROFEN (View Ketoprofen Review and Ketoprofen Label ), CIPROFLOXACIN HCL (View Ciprofloxacin Hcl Review and Ciprofloxacin Hcl Label ), SEVOFLURANE (View Sevoflurane Review and Sevoflurane Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), SUFENTANIL CITRATE (View Sufentanil Citrate Review and Sufentanil Citrate Label ), ETOMIDATE (View Etomidate Review and Etomidate Label ). Patient was hospitalized.

5213186-6 | Anaphylactic Shock, Carbon Dioxide Decreased, Circulatory Collapse, Face Oedema, Rash, Sinus Tachycardia
on Jan 17, 2007 Female patient from FRANCE , 45 years of age, was diagnosed with anaesthesia and was treated with Tracrium (View Usage). Patient had the following side effects: anaphylactic shock, carbon dioxide decreased, circulatory collapse, face oedema, rash (What is rash?), sinus tachycardia. Tracrium dosage: . During the same period patient was treated with CEFACIDAL (View Cefacidal Review and Cefacidal Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), SUFENTA (View Sufenta Review and Sufenta Label ), BLEU PATENTE (View Bleu Patente Review and Bleu Patente Label ), ACUPAN (View Acupan Review and Acupan Label ), SEVORANE (View Sevorane Review and Sevorane Label ), KETOPROFEN (View Ketoprofen Review and Ketoprofen Label ), PERFALGAN (View Perfalgan Review and Perfalgan Label ).

5207205-0 | Anaphylactic Shock, Carbon Dioxide Decreased, Circulatory Collapse, Face Oedema, Rash, Sinus Tachycardia
Patient was taking Tracrium (View Usage). After Tracrium was administered, patient had the following side effects: anaphylactic shock, carbon dioxide decreased, circulatory collapse, face oedema, rash (What is rash?), sinus tachycardia on Jan 08, 2007 from FRANCE Additional patient health information: Female patient , 45 years of age, was diagnosed with anaesthesia and. Tracrium dosage: . During the same period patient was treated with CEFACIDAL (View Cefacidal Review and Cefacidal Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), SUFENTA (View Sufenta Review and Sufenta Label ), BLEU PATENTE (View Bleu Patente Review and Bleu Patente Label ), ACUPAN (View Acupan Review and Acupan Label ), SEVORANE (View Sevorane Review and Sevorane Label ), KETOPROFEN (View Ketoprofen Review and Ketoprofen Label ), PERFALGAN (View Perfalgan Review and Perfalgan Label ).

5045216-9 | Cardiac Arrest, Respiratory Arrest, Shock, Tachycardia, Ventricular Fibrillation, Ventricular Tachycardia
Adverse event was reported on Jun 28, 2006 by a Male patient taking Tracrium (View Usage) (Dosage: ) . Location: FRANCE , 67 years of age, Patient experienced the following unwanted or unexpected effects: cardiac arrest (What is cardiac arrest?), respiratory arrest, shock, tachycardia, ventricular fibrillation, ventricular tachycardia. During the same period patient was treated with AUGMENTIN '125' (2g Single Dose) (View Augmentin '125' Review and Augmentin '125' Label ), HYPNOVEL (View Hypnovel Review and Hypnovel Label ), RAPIFEN (View Rapifen Review and Rapifen Label ), PROPOFOL (View Propofol Review and Propofol Label ).

5025187-1 | Erythema, Hypotension
on Apr 06, 2006 Male patient from FRANCE , 43 years of age, was diagnosed with induction of anaesthesia, antibiotic prophylaxis and was treated with Tracrium (View Usage). Patient had the following side effects: erythema, hypotension. Tracrium dosage: . During the same period patient was treated with HYPNOVEL (View Hypnovel Review and Hypnovel Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), CEFAZOLIN SODIUM (2g Per Day) (View Cefazolin Sodium Review and Cefazolin Sodium Label ), SUFENTA (View Sufenta Review and Sufenta Label ).

4966041-0 | Erythema, Hypotension
on Apr 06, 2006 Male patient from FRANCE , 43 years of age, was diagnosed with antibiotic prophylaxis and was treated with Tracrium (View Usage). After Tracrium was administered, patient had the following side effects: erythema, hypotension. Tracrium dosage: . During the same period patient was treated with HYPNOVEL (View Hypnovel Review and Hypnovel Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), CEFAZOLIN SODIUM (2g Per Day) (View Cefazolin Sodium Review and Cefazolin Sodium Label ), SUFENTA (View Sufenta Review and Sufenta Label ).

4932011-1 | Bronchospasm, Oxygen Saturation Decreased
Patient was taking Tracrium (View Usage). Patient experienced the following unwanted or unexpected effects: bronchospasm, oxygen saturation decreased on Feb 23, 2006 from FRANCE Additional patient health information: Male patient , 58 years of age, was diagnosed with anaesthesia and. Tracrium dosage: . During the same period patient was treated with ZINNAT INJECTABLE (View Zinnat Injectable Review and Zinnat Injectable Label ), HYPNOVEL (View Hypnovel Review and Hypnovel Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), SUFENTA (View Sufenta Review and Sufenta Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), OROCAL (View Orocal Review and Orocal Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), EUPANTOL (View Eupantol Review and Eupantol Label ). Patient was hospitalized.

4915310-9 | Anaphylactic Shock
Adverse event was reported on Jan 03, 2006 by a Male patient taking Tracrium (View Usage) (Dosage: ) . Location: FRANCE , 29 years of age, Patient had the following side effects: anaphylactic shock. During the same period patient was treated with CEFACIDAL (View Cefacidal Review and Cefacidal Label ), SUFENTA (View Sufenta Review and Sufenta Label ), PROPOFOL (View Propofol Review and Propofol Label ).

4883340-1 | Anaphylactic Shock
on Jan 03, 2006 Male patient from FRANCE , 29 years of age, was treated with Tracrium (View Usage). After Tracrium was administered, patient had the following side effects: anaphylactic shock. Tracrium dosage: . During the same period patient was treated with CEFACIDAL (View Cefacidal Review and Cefacidal Label ), SUFENTA (View Sufenta Review and Sufenta Label ), PROPOFOL (View Propofol Review and Propofol Label ).

4877579-9 | Anaphylactic Shock
on Jan 03, 2006 Male patient from FRANCE , 20 years of age, was treated with Tracrium (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock. Tracrium dosage: . During the same period patient was treated with CEFACIDAL (View Cefacidal Review and Cefacidal Label ), SUFENTA (View Sufenta Review and Sufenta Label ), PROPOFOL (View Propofol Review and Propofol Label ).

4877568-4 | Anaphylactic Shock, Erythema, Hypotension
Patient was taking Tracrium (View Usage). Patient had the following side effects: anaphylactic shock, erythema, hypotension on Jan 03, 2006 from FRANCE Additional patient health information: Male patient , 69 years of age, was diagnosed with anaesthesia and. Tracrium dosage: . During the same period patient was treated with ZINNAT INJECTABLE (View Zinnat Injectable Review and Zinnat Injectable Label ), ALFENTANIL (View Alfentanil Review and Alfentanil Label ), MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ). Patient was hospitalized.

4814638-0 | Anaphylactoid Reaction, Bronchospasm, Erythema, Hypotension, Tachycardia
Adverse event was reported on Oct 13, 2005 by a Male patient taking Tracrium (View Usage) (Dosage: ) . Location: FRANCE , 69 years of age, After Tracrium was administered, patient had the following side effects: anaphylactoid reaction, bronchospasm, erythema, hypotension, tachycardia. During the same period patient was treated with DIPRIVAN (View Diprivan Review and Diprivan Label ), SUFENTA (View Sufenta Review and Sufenta Label ), CEFAZOLIN SODIUM (View Cefazolin Sodium Review and Cefazolin Sodium Label ).

4679386-9 | Abdominal Pain, Alanine Aminotransferase Increased, Anaemia, Aspartate Aminotransferase Increased, Catheter Site Haemorrhage, Coma, Electroencephalogram Abnormal, Hepatocellular Damage, Hyperkalaemia
on May 19, 2005 Female patient from , weighting 20.72 lb, was treated with Tracrium (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, catheter site haemorrhage, coma, electroencephalogram abnormal, hepatocellular damage, hyperkalaemia. Tracrium dosage: 49mg Per Day. During the same period patient was treated with AUGMENTIN '125' (500mg Per Day) (View Augmentin '125' Review and Augmentin '125' Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), PERFALGAN (150mg Four Times Per Day) (View Perfalgan Review and Perfalgan Label ), SUFENTANIL (109mcg Per Day) (View Sufentanil Review and Sufentanil Label ), NUBAIN (26mg Per Day) (View Nubain Review and Nubain Label ), LEVOCARNIL (500mg Per Day) (View Levocarnil Review and Levocarnil Label ), MOTILIUM (View Motilium Review and Motilium Label ), SMECTA (1unit Per Day) (View Smecta Review and Smecta Label ).

4667795-3 | Mucosal Erosion, Stevens-johnson Syndrome, Toxic Epidermal Necrolysis
on Jul 26, 1999 Female patient from , 63 years of age, weighting 132.3 lb, was diagnosed with prophylaxis, sedation and was treated with Tracrium (View Usage). Patient had the following side effects: mucosal erosion, stevens-johnson syndrome, toxic epidermal necrolysis. Tracrium dosage: 2.5ml Single Dose. During the same period patient was treated with RANITIDINE (150mg Per Day) (View Ranitidine Review and Ranitidine Label ), DIPYRONE TAB (View Dipyrone Tab Review and Dipyrone Tab Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), OXAZEPAM (View Oxazepam Review and Oxazepam Label ). Patient was hospitalized.

4661461-6 | Mucosal Erosion, Stevens-johnson Syndrome, Toxic Epidermal Necrolysis
Patient was taking Tracrium (View Usage). After Tracrium was administered, patient had the following side effects: mucosal erosion, stevens-johnson syndrome, toxic epidermal necrolysis on Jul 26, 1999 from Additional patient health information: Female patient , 63 years of age, weighting 132.3 lb, was diagnosed with prophylaxis, sedation and. Tracrium dosage: 2.5ml Single Dose. During the same period patient was treated with RANITIDINE (150mg Per Day) (View Ranitidine Review and Ranitidine Label ), DIPYRONE TAB (View Dipyrone Tab Review and Dipyrone Tab Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), OXAZEPAM (View Oxazepam Review and Oxazepam Label ). Patient was hospitalized.

4629078-7 | Anaphylactic Shock, Bradycardia, Circulatory Collapse, Hypotension, Tachycardia
Adverse event was reported on Jan 31, 2005 by a Male patient taking Tracrium (View Usage) (Dosage: 260mg Single Dose) . Location: , 68 years of age, weighting 165.3 lb, Patient experienced the following unwanted or unexpected effects: anaphylactic shock, bradycardia, circulatory collapse, hypotension, tachycardia. During the same period patient was treated with ZINNAT INJECTABLE (1.5g Single Dose) (View Zinnat Injectable Review and Zinnat Injectable Label ), ACUPAN (20mg Single Dose) (View Acupan Review and Acupan Label ), KETAMINE HCL (View Ketamine Hcl Review and Ketamine Hcl Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), SUFENTA (40mcg Single Dose) (View Sufenta Review and Sufenta Label ), SOPROL (1tab Per Day) (View Soprol Review and Soprol Label ), PRETERAX (1tab Per Day) (View Preterax Review and Preterax Label ), ATARAX (100mg Single Dose) (View Atarax Review and Atarax Label ). Patient was hospitalized.


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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 Tracrium 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 Tracrium quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Tracrium 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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(View Fentanyl Review and Fentanyl Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), TRACRIUM (View Tracrium Review and Tracrium ... During the same period ...

During the same period patient was treated with TRACRIUM (View Tracrium Review and Tracrium Label ), ULTIVA (View Ultiva Review and Ultiva Label ), AUGMENTIN '125' (3 G Once ...

... Atarax Label ), SUFENTA PRESERVATIVE FREE (View Sufenta Preservative Free Review and Sufenta Preservative Free Label ), TRACRIUM (View Tracrium Review and Tracrium Label ), ...

Report a Drug Side Effect. ... This anonymous Drug Side Effect Survey has 13 questions and takes less than 2 minutes to complete.

During the same period patient was treated with AUGMENTIN '125', ACETAMINOPHEN, TRACRIUM, ETOMIDATE, LASIX, OFLOCET /00731801/, NICARDIPINE HCL ...

Had RhoGAM after childirth in 1972 and 1975. In 1992 I was diagnosed ... Tracrium Side Effects... LEVOCARNIL (500mg Per Day) (View Levocarnil Review and Levocarnil Label ...

... Nimbex Review and Nimbex Label ), TETANUS VACCINE (1 Per Day) (View Tetanus Vaccine Review and Tetanus Vaccine Label ), TRACRIUM (View Tracrium Review and Tracrium Label ), ...

During the same period patient was treated with TRACRIUM (35mg Per Day) (View Tracrium Review and Tracrium Label ), MIDAZOLAM HCL (1mg Per Day) (View Midazolam Hcl Review and ...

tracrium Episodes: 2: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: tranxilium Episodes: 1: Diagnosed with major depression.Side ...

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Tracrium Reactions
Abdominal PainWhat is Abdominal pain?
Agitation
Alanine Aminotransferase Increased
Anaemia
Anaphylactic Shock
Anaphylactoid Reaction
Aspartate Aminotransferase Increased
Bradycardia
Bronchospasm
C-reactive Protein Increased
Carbon Dioxide Decreased
Cardiac ArrestWhat is Cardiac arrest?
Circulatory Collapse
Dermatomyositis
Dyspnoea
Erythema
Face Oedema
Hypotension
Leg Amputation
Lung Disorder
Lymphocele
Lymphopenia
Mucosal Erosion
Neoplasm
RashWhat is Rash?
Rash Erythematous
Sinus Tachycardia
Stevens-johnson Syndrome
Tachycardia
Toxic Epidermal Necrolysis
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