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Summary

FDA Adverse Reports: 185. View All

Tavor FDA safety alerts: No

Reported deaths: 9

Reported hospitalizations: 171

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

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5078669-0 | Somnolence, Suicide Attempt, Tachycardia
on Jul 24, 2006 Female patient from GERMANY , 34 years of age, was treated with Tavor (View Usage). Patient experienced the following unwanted or unexpected effects: somnolence, suicide attempt, tachycardia. Tavor dosage: 4 Mg Once Po. During the same period patient was treated with ZOPICLONE (75 Mg Once Po) (View Zopiclone Review and Zopiclone Label ). Patient was hospitalized.

5076071-9 | Coma, Hypertension, Respiratory Depression, Somnolence, Tachycardia
Patient was taking Tavor (View Usage). Patient had the following side effects: coma, hypertension, respiratory depression, somnolence, tachycardia on Jul 19, 2006 from GERMANY Additional patient health information: Male patient , 73 years of age, . Tavor dosage: . During the same period patient was treated with OXYCODONE HCL (40 Mg Once; Po) (View Oxycodone Hcl Review and Oxycodone Hcl Label ). Patient was hospitalized.

5053307-1 | Abnormal Behaviour, Delirium, Delusion, Disorientation, Disturbance In Attention, Memory Impairment, Sleep Disorder, Thinking Abnormal
Adverse event was reported on Jun 26, 2006 by a Male patient taking Tavor (View Usage) (Dosage: 0.5 Mg Po) was diagnosed with depression (What is depression?) and. Location: GERMANY , 50 years of age, After Tavor was administered, patient had the following side effects: abnormal behaviour, delirium, delusion, disorientation, disturbance in attention, memory impairment, sleep disorder (What is sleep disorder?), thinking abnormal. During the same period patient was treated with VENLAFAXINE HCL (Var Po) (View Venlafaxine Hcl Review and Venlafaxine Hcl Label ). Patient was hospitalized.

5053302-2 | Coma, Cyanosis, Hypotension, Suicide Attempt
on Jun 26, 2006 Female patient from GERMANY , 65 years of age, was treated with Tavor (View Usage). Patient experienced the following unwanted or unexpected effects: coma, cyanosis, hypotension, suicide attempt. Tavor dosage: Dr Once Po. During the same period patient was treated with DALMADORM (Df Once Po) (View Dalmadorm Review and Dalmadorm Label ), TRICYCLIC ANTIDEPRESSANTS (Df Once Po) (View Tricyclic Antidepressants Review and Tricyclic Antidepressants Label ), PERAZINE (Df Once Po) (View Perazine Review and Perazine Label ), ALCOHOL (500 Ml Once Po) (View Alcohol Review and Alcohol Label ). Patient was hospitalized.


5053301-0 | Arrhythmia, Cardiac Failure, Cardiac Valve Disease, Deep Vein Thrombosis, Infection, Pulmonary Embolism, Sepsis
on Jun 26, 2006 Male patient from GERMANY , 39 years of age, was treated with Tavor (View Usage). Patient had the following side effects: arrhythmia (What is arrhythmia?), cardiac failure, cardiac valve disease, deep vein thrombosis (What is deep vein thrombosis?), infection (What is infection?), pulmonary embolism (What is pulmonary embolism?), sepsis (What is sepsis?). Tavor dosage: 3 Mg Qd Po. During the same period patient was treated with ZYPREXA (20 Mg Qd Po) (View Zyprexa Review and Zyprexa Label ), POLAMIDON (View Polamidon Review and Polamidon Label ), LANITOP (View Lanitop Review and Lanitop Label ), ISOKET (View Isoket Review and Isoket Label ), HCT (View Hct Review and Hct Label ).

5053273-9 | Back Pain, Deep Vein Thrombosis, Pain In Extremity, Pneumonia, Pulmonary Embolism, Pulmonary Infarction, Sedation
Patient was taking Tavor (View Usage). After Tavor was administered, patient had the following side effects: back pain (What is back pain?), deep vein thrombosis (What is deep vein thrombosis?), pain in extremity, pneumonia (What is pneumonia?), pulmonary embolism (What is pulmonary embolism?), pulmonary infarction, sedation on Jun 26, 2006 from GERMANY Additional patient health information: Female patient , 38 years of age, . Tavor dosage: 7.5 Mg Q Day Po. During the same period patient was treated with HALDOL (20 Mg Q Day Po) (View Haldol Review and Haldol Label ), AKINETON (View Akineton Review and Akineton Label ), JODTHYROX (View Jodthyrox Review and Jodthyrox Label ). Patient was hospitalized.

5050532-0 | Abdominal Pain Upper, Intentional Overdose, Suicide Attempt
Adverse event was reported on Jun 22, 2006 by a Female patient taking Tavor (View Usage) (Dosage: 80 Mg Once Po) . Location: GERMANY , 47 years of age, Patient experienced the following unwanted or unexpected effects: abdominal pain upper, intentional overdose, suicide attempt. During the same period patient was treated with DRAIN PIPE CLEANER (5 Ml Once) (View Drain Pipe Cleaner Review and Drain Pipe Cleaner Label ). Patient was hospitalized.

5048547-1 | Hallucination, Prothrombin Time Prolonged
on Jun 16, 2006 Female patient from GERMANY , 68 years of age, was treated with Tavor (View Usage). Patient had the following side effects: hallucination, prothrombin time prolonged. Tavor dosage: Df Once Po. During the same period patient was treated with MARCUMAR (Df) (View Marcumar Review and Marcumar Label ), SAROTEN (Df Once Po) (View Saroten Review and Saroten Label ), ADUMBRAN (10 Mg Q Day Po) (View Adumbran Review and Adumbran Label ), METOPROLOL (50 Mg Bid Po) (View Metoprolol Review and Metoprolol Label ), RAMIPRIL (2.5 Mg Q Day Po) (View Ramipril Review and Ramipril Label ), MST (30 Mg Bid Po) (View Mst Review and Mst Label ). Patient was hospitalized.

5042637-5 | Coma, Cyanosis, Hypotension, Suicide Attempt
on Jun 09, 2006 Female patient from GERMANY , 65 years of age, was treated with Tavor (View Usage). After Tavor was administered, patient had the following side effects: coma, cyanosis, hypotension, suicide attempt. Tavor dosage: Df Once Po. During the same period patient was treated with DALMADORM (Df Once Po) (View Dalmadorm Review and Dalmadorm Label ), TRICYCLIC ANTIDEPRESSANTS (Df Once Po) (View Tricyclic Antidepressants Review and Tricyclic Antidepressants Label ). Patient was hospitalized.

5036868-8 | Intentional Overdose, Mydriasis, Somnolence
Patient was taking Tavor (View Usage). Patient experienced the following unwanted or unexpected effects: intentional overdose, mydriasis, somnolence on Jun 08, 2006 from GERMANY Additional patient health information: Male patient , 26 years of age, . Tavor dosage: 80 Mg Once Po. Patient was hospitalized.

5036531-3 | Fatigue, Feeling Drunk, Tachycardia
Adverse event was reported on Jun 09, 2006 by a Female patient taking Tavor (View Usage) (Dosage: 2 Mg Once Po) . Location: GERMANY , 29 years of age, Patient had the following side effects: fatigue, feeling drunk, tachycardia. During the same period patient was treated with TRAMADOL HCL (200 Mg Once Po) (View Tramadol Hcl Review and Tramadol Hcl Label ), BOTTLE OF SPARKLING WINE (1 Bottle Once Po) (View Bottle Of Sparkling Wine Review and Bottle Of Sparkling Wine Label ). Patient was hospitalized.

5036520-9 | Somnolence, Suicide Attempt, Tachycardia
on Jun 09, 2006 Male patient from GERMANY , 24 years of age, was treated with Tavor (View Usage). After Tavor was administered, patient had the following side effects: somnolence, suicide attempt, tachycardia. Tavor dosage: Df Once Po. During the same period patient was treated with AKINETON /00079502/ (Df Once Po) (View Akineton /00079502/ Review and Akineton /00079502/ Label ), CHLORAL HYDRATE (Df Once Po) (View Chloral Hydrate Review and Chloral Hydrate Label ), FORADIL (Df Once Po) (View Foradil Review and Foradil Label ), GLIANIMON (Df Once Po) (View Glianimon Review and Glianimon Label ), NEUROCIL /00038602/ (Df Once Po) (View Neurocil /00038602/ Review and Neurocil /00038602/ Label ), NIPOLEPT (Df Once Po) (View Nipolept Review and Nipolept Label ), THEOPHYLLINE (Df Once Po) (View Theophylline Review and Theophylline Label ). Patient was hospitalized.

5022369-X | Convulsion, Disorientation, Fall, Hyponatraemia, Loss Of Consciousness, Polydipsia, Vomiting
on May 19, 2006 Female patient from GERMANY , 49 years of age, was treated with Tavor (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion, disorientation, fall (What is fall?), hyponatraemia, loss of consciousness, polydipsia, vomiting. Tavor dosage: 0.5 Mg Q Day Po. During the same period patient was treated with ZYPREXA (20 Mg Q Day Po) (View Zyprexa Review and Zyprexa Label ). Patient was hospitalized.

5019535-6 | Blood Pressure Decreased, Blood Pressure Systolic Increased, Heart Rate Decreased, Syncope
Patient was taking Tavor (View Usage). Patient had the following side effects: blood pressure decreased, blood pressure systolic increased, heart rate decreased, syncope on May 12, 2006 from GERMANY Additional patient health information: Female patient , 21 years of age, weighting 114.2 lb, was diagnosed with depression (What is depression?), suicidal ideation and. Tavor dosage: 2 Mg Q Day Po. During the same period patient was treated with NEUROCIL /00038602/ (50 Mg Once) (View Neurocil /00038602/ Review and Neurocil /00038602/ Label ), ZOLOFT (View Zoloft Review and Zoloft Label ). Patient was hospitalized.

5011557-4 | Diarrhoea, Intentional Overdose, Mydriasis, Somnolence
Adverse event was reported on May 08, 2006 by a Male patient taking Tavor (View Usage) (Dosage: 80 Mg Once Po) . Location: GERMANY , 26 years of age, After Tavor was administered, patient had the following side effects: diarrhoea, intentional overdose, mydriasis, somnolence. Patient was hospitalized.

5011556-2 | Diarrhoea, Dry Mouth, Fatigue, Intentional Overdose, Suicide Attempt
on May 08, 2006 Male patient from GERMANY , 41 years of age, was treated with Tavor (View Usage). Patient experienced the following unwanted or unexpected effects: diarrhoea, dry mouth, fatigue, intentional overdose, suicide attempt. Tavor dosage: 10 Mg Once Po. Patient was hospitalized.

5006971-7 | Somnolence, Suicide Attempt, Tachycardia
on May 01, 2006 Male patient from GERMANY , 24 years of age, was treated with Tavor (View Usage). Patient had the following side effects: somnolence, suicide attempt, tachycardia. Tavor dosage: Df Once Po. During the same period patient was treated with AKINETON (Df Once Po) (View Akineton Review and Akineton Label ), CHLORAL HYDRATE (Df Once Po) (View Chloral Hydrate Review and Chloral Hydrate Label ), FORADIL (Df Once Po) (View Foradil Review and Foradil Label ), GLIANIMON (Df Once Po) (View Glianimon Review and Glianimon Label ), NEUROCIL (Df Once Po) (View Neurocil Review and Neurocil Label ), NIPOLEPT (Df Once Po) (View Nipolept Review and Nipolept Label ), THEOPHYLLINE (Df Once Po) (View Theophylline Review and Theophylline Label ), ZELDOX (Df Once Po) (View Zeldox Review and Zeldox Label ). Patient was hospitalized.

5002621-4 | Blood Alcohol Increased, Suicide Attempt, Vomiting
Patient was taking Tavor (View Usage). After Tavor was administered, patient had the following side effects: blood alcohol increased, suicide attempt, vomiting on Apr 24, 2006 from GERMANY Additional patient health information: Female patient , 30 years of age, . Tavor dosage: 10 Mg Once Po. During the same period patient was treated with MIRTAZAPINE (150 Mg Once Po) (View Mirtazapine Review and Mirtazapine Label ), VENLAFAXINE HCL (525 Mg Once Po) (View Venlafaxine Hcl Review and Venlafaxine Hcl Label ), ZYBAN (Df Once Po) (View Zyban Review and Zyban Label ), ALCOHOL (Df Once Po) (View Alcohol Review and Alcohol Label ). Patient was hospitalized.

4999927-1 | Blood Alcohol Increased, Overdose, Pupillary Reflex Impaired, Suicide Attempt
Adverse event was reported on Apr 24, 2006 by a Female patient taking Tavor (View Usage) (Dosage: 5 Mg Once Po) . Location: GERMANY , 40 years of age, Patient experienced the following unwanted or unexpected effects: blood alcohol increased, overdose, pupillary reflex impaired, suicide attempt. During the same period patient was treated with AMITRIPTYLINE HCL (Df Once Po) (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), ALCOHOL (Df Once Po) (View Alcohol Review and Alcohol Label ). Patient was hospitalized.

4998652-0 | Depressed Level Of Consciousness, Intentional Overdose, Mydriasis, Suicide Attempt
on Apr 21, 2006 Male patient from GERMANY , 33 years of age, was treated with Tavor (View Usage). Patient had the following side effects: depressed level of consciousness, intentional overdose, mydriasis, suicide attempt. Tavor dosage: 20 Mg Once Po. During the same period patient was treated with STILNOX (170 Mg Once Po) (View Stilnox Review and Stilnox Label ). Patient was hospitalized.

4989789-0 | Flushing, Pyrexia, Tremor
on Apr 14, 2006 Female patient from GERMANY , 44 years of age, was treated with Tavor (View Usage). After Tavor was administered, patient had the following side effects: flushing, pyrexia, tremor. Tavor dosage: 1 Mg Q Day Po. During the same period patient was treated with ATOSIL (100 Mg Q Day Po) (View Atosil Review and Atosil Label ), JATROSOM (1 Tab Q Day Po) (View Jatrosom Review and Jatrosom Label ). Patient was hospitalized.

4987835-1 | Depressed Level Of Consciousness, Mydriasis, Overdose, Suicide Attempt
Patient was taking Tavor (View Usage). Patient experienced the following unwanted or unexpected effects: depressed level of consciousness, mydriasis, overdose, suicide attempt on Apr 10, 2006 from GERMANY Additional patient health information: Male patient , 33 years of age, . Tavor dosage: 20 Mg Once Po. During the same period patient was treated with STILNOX (170 Mg Once Po) (View Stilnox Review and Stilnox Label ). Patient was hospitalized.

4984544-X | Blood Pressure Decreased, Dizziness, Fall, Syncope, Vomiting
Adverse event was reported on Apr 05, 2006 by a Female patient taking Tavor (View Usage) (Dosage: 1.5 Mg Q Day Po) . Location: GERMANY , 24 years of age, Patient had the following side effects: blood pressure decreased, dizziness (What is dizziness?), fall (What is fall?), syncope, vomiting. During the same period patient was treated with ABILIFY (15 Mg Q Day Po) (View Abilify Review and Abilify Label ), ZELDOX (View Zeldox Review and Zeldox Label ), SOLIAN (View Solian Review and Solian Label ). Patient was hospitalized.

4978824-1 | Fatigue, Intentional Overdose, Suicide Attempt, Tachycardia
on Mar 31, 2006 Female patient from GERMANY , 44 years of age, was treated with Tavor (View Usage). After Tavor was administered, patient had the following side effects: fatigue, intentional overdose, suicide attempt, tachycardia. Tavor dosage: 5 Mg Once Po.

4978414-0 | Respiratory Failure, Salivary Hypersecretion, Somnolence
on Mar 31, 2006 Male patient from GERMANY , 48 years of age, was treated with Tavor (View Usage). Patient experienced the following unwanted or unexpected effects: respiratory failure, salivary hypersecretion, somnolence. Tavor dosage: Df Once. During the same period patient was treated with CLOZAPINE (Df Once) (View Clozapine Review and Clozapine Label ). Patient was hospitalized.

4977403-X | Apathy, Depressed Level Of Consciousness, Suicide Attempt
Patient was taking Tavor (View Usage). Patient had the following side effects: apathy, depressed level of consciousness, suicide attempt on Mar 28, 2006 from GERMANY Additional patient health information: Female patient , 45 years of age, . Tavor dosage: 6 Mg Once Po. During the same period patient was treated with DIAZEPAM (100 Mg Once Po) (View Diazepam Review and Diazepam Label ), CIATYL /00075802/ (2 Ml Q Day Po) (View Ciatyl /00075802/ Review and Ciatyl /00075802/ Label ), HALDOL (80 Gtt Q Day Po) (View Haldol Review and Haldol Label ), NEUROCIL /00038602/ (150 Gtt Q Day Po) (View Neurocil /00038602/ Review and Neurocil /00038602/ Label ). Patient was hospitalized.

4964885-2 | Sopor, Suicide Attempt, Tachycardia
Adverse event was reported on Mar 16, 2006 by a Female patient taking Tavor (View Usage) (Dosage: Df Once, Po) . Location: GERMANY , 37 years of age, After Tavor was administered, patient had the following side effects: sopor, suicide attempt, tachycardia. During the same period patient was treated with IBUPROFEN (Df Once, Po) (View Ibuprofen Review and Ibuprofen Label ), LASIX (Df Once, Po) (View Lasix Review and Lasix Label ), TALVOSILEN (Df Once, Po) (View Talvosilen Review and Talvosilen Label ), ALCOHOL (Df Once, Po) (View Alcohol Review and Alcohol Label ), RAT POISON (Dr Once) (View Rat Poison Review and Rat Poison Label ). Patient was hospitalized.

4954531-6 | Arterial Injury, Coma, Injury Asphyxiation, Suicide Attempt, Tachycardia
on Mar 06, 2006 Female patient from GERMANY , 36 years of age, was treated with Tavor (View Usage). Patient experienced the following unwanted or unexpected effects: arterial injury, coma, injury asphyxiation, suicide attempt, tachycardia. Tavor dosage: Df Once Po. During the same period patient was treated with SEROQUEL (Df Once Po) (View Seroquel Review and Seroquel Label ), TRUXAL (Df Once Po) (View Truxal Review and Truxal Label ). Patient was hospitalized.

4950950-2 | Bradycardia, Suicide Attempt
on Feb 27, 2006 Female patient from GERMANY , 38 years of age, was treated with Tavor (View Usage). Patient had the following side effects: bradycardia, suicide attempt. Tavor dosage: 100 Mg Once Po. During the same period patient was treated with FLUCTIN (1000 Mg Once Po) (View Fluctin Review and Fluctin Label ), JATROSOM (450 Mg Once Po) (View Jatrosom Review and Jatrosom Label ). Patient was hospitalized.

4950949-6 | Alcohol Use, Intentional Overdose, Somnolence, Sopor, Suicide Attempt, Tachycardia
Patient was taking Tavor (View Usage). After Tavor was administered, patient had the following side effects: alcohol use, intentional overdose, somnolence, sopor, suicide attempt, tachycardia on Feb 27, 2006 from GERMANY Additional patient health information: Female patient , 22 years of age, . Tavor dosage: 10 Mg Once Po. During the same period patient was treated with VENLAFAXINE HCL (2000 Mg Once Po) (View Venlafaxine Hcl Review and Venlafaxine Hcl Label ), SEROQUEL (2000 Mg Once Po) (View Seroquel Review and Seroquel Label ), BEER/WINE (1 Bottle Once Po) (View Beer/wine Review and Beer/wine Label ). Patient was hospitalized.

4950159-2 | Dizziness, Nausea, Suicide Attempt
Adverse event was reported on Feb 28, 2006 by a Female patient taking Tavor (View Usage) (Dosage: 20 Mg Once Po) . Location: GERMANY , 24 years of age, Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), nausea (What is nausea?), suicide attempt. During the same period patient was treated with FLUOXETINE HCL (Df Once Po) (View Fluoxetine Hcl Review and Fluoxetine Hcl Label ), PAROXETINE (80 Mg Once Po) (View Paroxetine Review and Paroxetine Label ). Patient was hospitalized.

4948418-2 | Acidosis, Acute Respiratory Distress Syndrome, Aspiration, Colonic Atony, Coma, Pco2 Increased, Suicide Attempt, Tachycardia
on Feb 23, 2006 Male patient from GERMANY , 31 years of age, was treated with Tavor (View Usage). Patient had the following side effects: acidosis, acute respiratory distress syndrome, aspiration, colonic atony, coma, pco2 increased, suicide attempt, tachycardia. Tavor dosage: Df, Once; Po. During the same period patient was treated with AMITRYPTYLINE (Df Once; Po) (View Amitryptyline Review and Amitryptyline Label ), BROMAZANIL (Df Once; Po) (View Bromazanil Review and Bromazanil Label ), DIAZEPAM (Df Once; Po) (View Diazepam Review and Diazepam Label ), DOXEPIN (Df Once; Po) (View Doxepin Review and Doxepin Label ), OXAZEPAM (Df Once; Po) (View Oxazepam Review and Oxazepam Label ), MIRTAZAPINE (Df Once, Po) (View Mirtazapine Review and Mirtazapine Label ), STANGYL /00051802/ (Df Once; Po) (View Stangyl /00051802/ Review and Stangyl /00051802/ Label ), TRANXILLIUM (Df Once; Po) (View Tranxillium Review and Tranxillium Label ). Patient was hospitalized.

4932421-2 | Dizziness, Intentional Overdose, Nausea, Self-induced Vomiting, Suicide Attempt
on Feb 13, 2006 Female patient from GERMANY , 24 years of age, was treated with Tavor (View Usage). After Tavor was administered, patient had the following side effects: dizziness (What is dizziness?), intentional overdose, nausea (What is nausea?), self-induced vomiting, suicide attempt. Tavor dosage: 20 Mg Once Po. During the same period patient was treated with FLUOXETINE HCL (Df Once Po) (View Fluoxetine Hcl Review and Fluoxetine Hcl Label ), PAROXETINE HCL (100 Mg Once Po) (View Paroxetine Hcl Review and Paroxetine Hcl Label ). Patient was hospitalized.

4929508-7 | Fatigue, Suicide Attempt, Tachycardia
Patient was taking Tavor (View Usage). Patient experienced the following unwanted or unexpected effects: fatigue, suicide attempt, tachycardia on Feb 08, 2006 from GERMANY Additional patient health information: Female patient , 19 years of age, . Tavor dosage: 7.5 Mg Once Po. During the same period patient was treated with NEUROCIL (325 Mg Once Po) (View Neurocil Review and Neurocil Label ), SEROQUEL (1000 Mg Once Po) (View Seroquel Review and Seroquel Label ).

4928167-7 | Neonatal Infection, Neonatal Respiratory Failure
Adverse event was reported on Feb 07, 2006 by a Female patient taking Tavor (View Usage) (Dosage: Df Q Day Tran-p) . Location: GERMANY , weighting 9.59 lb, Patient had the following side effects: neonatal infection, neonatal respiratory failure. During the same period patient was treated with TREVILOR SLOW RELEASE (75 Mg Qid Tran-p) (View Trevilor - Slow Release Review and Trevilor - Slow Release Label ), ABILIFY (View Abilify Review and Abilify Label ), ZYPREXA (View Zyprexa Review and Zyprexa Label ). Patient was hospitalized.

4921179-9 | Fatigue, Intentional Overdose, Suicide Attempt, Tachycardia
on Feb 03, 2006 Female patient from GERMANY , 42 years of age, was treated with Tavor (View Usage). After Tavor was administered, patient had the following side effects: fatigue, intentional overdose, suicide attempt, tachycardia. Tavor dosage: 3 Mg Once Po. During the same period patient was treated with ZOLPIDEM (20 Mg Once Po) (View Zolpidem Review and Zolpidem Label ). Patient was hospitalized.

4920685-0 | Alcohol Use, Gait Disturbance, Intentional Overdose, Mydriasis, Somnolence, Suicide Attempt, Tachycardia
on Jan 31, 2006 Female patient from GERMANY , 36 years of age, was treated with Tavor (View Usage). Patient experienced the following unwanted or unexpected effects: alcohol use, gait disturbance, intentional overdose, mydriasis, somnolence, suicide attempt, tachycardia. Tavor dosage: 1 Mg Once Po. During the same period patient was treated with CHLORPROTHIXENE (150 Mg Once Po) (View Chlorprothixene Review and Chlorprothixene Label ), DIAZEPAM (Df Once Po) (View Diazepam Review and Diazepam Label ), ALCOHOL (Df Po) (View Alcohol Review and Alcohol Label ). Patient was hospitalized.

4913391-X | Arrhythmia, Coma, Suicide Attempt, Tachycardia
Patient was taking Tavor (View Usage). Patient had the following side effects: arrhythmia (What is arrhythmia?), coma, suicide attempt, tachycardia on Jan 26, 2006 from GERMANY Additional patient health information: Female patient , 22 years of age, . Tavor dosage: 5 Mg Once Po. During the same period patient was treated with SEROQUEL (400 Mg Once Po) (View Seroquel Review and Seroquel Label ), STANCYL (Df Once Po) (View Stancyl Review and Stancyl Label ). Patient was hospitalized.

4907935-1 | Blood Potassium Increased, Overdose, Somnolence, Suicide Attempt
Adverse event was reported on Jan 23, 2006 by a Female patient taking Tavor (View Usage) (Dosage: 50 Mg Once Po) . Location: GERMANY , 56 years of age, After Tavor was administered, patient had the following side effects: blood potassium increased, overdose, somnolence, suicide attempt. Patient was hospitalized.

4906856-8 | Intentional Overdose, Suicide Attempt, Tachycardia
on Jan 23, 2006 Male patient from GERMANY , 39 years of age, was treated with Tavor (View Usage). Patient experienced the following unwanted or unexpected effects: intentional overdose, suicide attempt, tachycardia. Tavor dosage: 10 Mg Once Po. Patient was hospitalized.

4851107-6 | Miosis, Sopor, Suicide Attempt
on Nov 21, 2005 Female patient from GERMANY , 19 years of age, was treated with Tavor (View Usage). Patient had the following side effects: miosis, sopor, suicide attempt. Tavor dosage: 10 Mg Once Po. During the same period patient was treated with MIRTAZAPINE (450 Mg Once Po) (View Mirtazapine Review and Mirtazapine Label ), ZOPICLONE (150 Mg Once Po) (View Zopiclone Review and Zopiclone Label ), ALCOHOL (Df Unk Po) (View Alcohol Review and Alcohol Label ). Patient was hospitalized.

4845861-7 | Amnesia, Bowel Sounds Abnormal, Coma, Mydriasis, Respiratory Failure, Strabismus, Tachycardia, Vomiting
Patient was taking Tavor (View Usage). After Tavor was administered, patient had the following side effects: amnesia, bowel sounds abnormal, coma, mydriasis, respiratory failure, strabismus, tachycardia, vomiting on Nov 15, 2005 from GERMANY Additional patient health information: Male patient , 43 years of age, . Tavor dosage: 20 Mg Once Po. During the same period patient was treated with STANGYL (10 G Once Po) (View Stangyl Review and Stangyl Label ), STILNOX (9 Tab Once Po) (View Stilnox Review and Stilnox Label ), THOMBRAN (1000 Mg Once Po) (View Thombran Review and Thombran Label ). Patient was hospitalized.

4844949-4 | Fatigue, Intentional Overdose, Tachycardia
Adverse event was reported on Nov 08, 2005 by a Female patient taking Tavor (View Usage) (Dosage: 15 Mg Once Po) . Location: GERMANY , 14 years of age, Patient experienced the following unwanted or unexpected effects: fatigue, intentional overdose, tachycardia. During the same period patient was treated with NOVALGIN /SCH/ (Df Once Po) (View Novalgin /sch/ Review and Novalgin /sch/ Label ). Patient was hospitalized.

4837404-9 | Supraventricular Extrasystoles, Tachycardia
on Nov 09, 2005 Female patient from GERMANY , 56 years of age, was treated with Tavor (View Usage). Patient had the following side effects: supraventricular extrasystoles, tachycardia. Tavor dosage: 1.25 Mg Q Day. During the same period patient was treated with EDRONAX (8 Mg Q Day) (View Edronax Review and Edronax Label ), RISPERDAL (Df) (View Risperdal Review and Risperdal Label ), DETROL (View Detrol Review and Detrol Label ), DECORTIN H (View Decortin-h Review and Decortin-h Label ). Patient was hospitalized.

4832030-X | Depressed Level Of Consciousness, Dry Mouth, Intentional Overdose, Tremor
on Oct 10, 2005 Female patient from GERMANY , 53 years of age, was treated with Tavor (View Usage). After Tavor was administered, patient had the following side effects: depressed level of consciousness, dry mouth, intentional overdose, tremor. Tavor dosage: . During the same period patient was treated with VENLAFAXINE HCL (3000 Mg Once Po) (View Venlafaxine Hcl Review and Venlafaxine Hcl Label ). Patient was hospitalized.

4831152-7 | Bowel Sounds Abnormal, Fatigue, Tachycardia
Patient was taking Tavor (View Usage). Patient experienced the following unwanted or unexpected effects: bowel sounds abnormal, fatigue, tachycardia on Sep 28, 2005 from GERMANY Additional patient health information: Female patient , 41 years of age, . Tavor dosage: 7 Mg Once Po. During the same period patient was treated with ATOSIL (1600 Mg Once Po) (View Atosil Review and Atosil Label ), LEPONEX (1000 Mg Once Po) (View Leponex Review and Leponex Label ). Patient was hospitalized.

4830550-5 | Alcohol Use, Coma, Sopor, Tachycardia
Adverse event was reported on Oct 05, 2005 by a Male patient taking Tavor (View Usage) (Dosage: 125 Mg Once) . Location: GERMANY , 29 years of age, Patient had the following side effects: alcohol use, coma, sopor, tachycardia. During the same period patient was treated with PHENCYCLIDINE (Df Once) (View Phencyclidine Review and Phencyclidine Label ), SUBUTEX (Df Once) (View Subutex Review and Subutex Label ), ALCOHOL (Df Once) (View Alcohol Review and Alcohol Label ). Patient was hospitalized.

4825436-6 | Agitation, Restlessness
on Oct 25, 2005 Female patient from GERMANY , 69 years of age, was treated with Tavor (View Usage). After Tavor was administered, patient had the following side effects: agitation, restlessness. Tavor dosage: 1 Mg Bid Po. During the same period patient was treated with ERGENYL CHRONO (600 Mg Po) (View Ergenyl Chrono Review and Ergenyl Chrono Label ), LAMICTAL (400 Mg Po) (View Lamictal Review and Lamictal Label ), ZYPREXA (5 Mg Q Day Po) (View Zyprexa Review and Zyprexa Label ). Patient was hospitalized.

4819040-3 | Fatigue, Tachycardia
on Oct 18, 2005 Female patient from GERMANY , 14 years of age, was treated with Tavor (View Usage). Patient experienced the following unwanted or unexpected effects: fatigue, tachycardia. Tavor dosage: 15 Mg Once Po. During the same period patient was treated with NOVALGIN /SCH/ (Df Once Po) (View Novalgin /sch/ Review and Novalgin /sch/ Label ). Patient was hospitalized.

4819034-8 | Bundle Branch Block Right, Coma, Sinus Tachycardia, Vertigo
Patient was taking Tavor (View Usage). Patient had the following side effects: bundle branch block right, coma, sinus tachycardia, vertigo on Oct 18, 2005 from GERMANY Additional patient health information: Female patient , 42 years of age, . Tavor dosage: 25 Mg Once Po. During the same period patient was treated with ALCOHOL (View Alcohol Review and Alcohol 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 Tavor 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 Tavor quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Tavor 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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Tavor Reactions
Accidental Overdose
Agitation
Alcohol Use
Aspartate Aminotransferase Increased
Blood Creatine Phosphokinase Increased
Bowel Sounds Abnormal
Bradycardia
Coma
Cyanosis
Depressed Level Of Consciousness
Diarrhoea
DizzinessWhat is Dizziness?
Dry Mouth
FallWhat is Fall?
Fatigue
Hallucination
Hypotension
Intentional Misuse
Intentional Overdose
Miosis
Mydriasis
NauseaWhat is Nausea?
Overdose
Respiratory Depression
Respiratory Failure
Somnolence
Sopor
Suicide Attempt
Tachycardia
Vomiting
Tavor 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 Tavor 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!