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FDA Adverse Reports: 400. View All

Ultram FDA safety alerts: No

Reported deaths: 35

Reported hospitalizations: 155

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

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6681026-4 | Poisoning, Unresponsive To Stimuli
on Apr 09, 2010 Female patient from UNITED STATES , 48 years of age, was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: poisoning (What is poisoning?), unresponsive to stimuli. Ultram dosage: . During the same period patient was treated with BACLOFEN (View Baclofen Review and Baclofen Label ), ETHANOL (View Ethanol Review and Ethanol Label ).

6681019-7 | Blood Pressure Increased, Confusional State, Convulsion, Nystagmus, Overdose
Patient was taking Ultram (View Usage). Patient had the following side effects: blood pressure increased, confusional state, convulsion, nystagmus, overdose on Apr 09, 2010 from UNITED STATES Additional patient health information: Male patient , 43 years of age, . Ultram dosage: . During the same period patient was treated with SOMA (View Soma Review and Soma Label ), COCAINE (View Cocaine Review and Cocaine Label ), ANTICONVULSANT (NOS) (View Anticonvulsant (nos) Review and Anticonvulsant (nos) Label ), CORTICOSTEROID (View Corticosteroid Review and Corticosteroid Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ).

6681018-5 | Convulsion, Mydriasis, Somnolence, Tachycardia
Adverse event was reported on Apr 09, 2010 by a Female patient taking Ultram (View Usage) (Dosage: ) . Location: UNITED STATES , 16 years of age, After Ultram was administered, patient had the following side effects: convulsion, mydriasis, somnolence, tachycardia. During the same period patient was treated with CYCLOBENZAPRINE (View Cyclobenzaprine Review and Cyclobenzaprine Label ).

6680990-7 | Body Temperature Decreased, Convulsion, Overdose, Pneumonia Aspiration, Respiratory Rate Decreased
on Apr 09, 2010 Male patient from UNITED STATES , 19 years of age, was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: body temperature decreased, convulsion, overdose, pneumonia aspiration, respiratory rate decreased. Ultram dosage: .


6680973-7 | Blood Amylase Increased, Blood Creatine Phosphokinase Increased, Hepatic Enzyme Increased, Hypothermia, International Normalised Ratio Increased, Overdose, Renal Failure Acute, Unresponsive To Stimuli
on Apr 09, 2010 Female patient from UNITED STATES , 57 years of age, was treated with Ultram (View Usage). Patient had the following side effects: blood amylase increased, blood creatine phosphokinase increased, hepatic enzyme increased, hypothermia (What is hypothermia?), international normalised ratio increased, overdose, renal failure acute, unresponsive to stimuli. Ultram dosage: . During the same period patient was treated with ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), ESTROGEN (View Estrogen Review and Estrogen Label ).

6680972-5 | Unresponsive To Stimuli
Patient was taking Ultram (View Usage). After Ultram was administered, patient had the following side effects: unresponsive to stimuli on Apr 09, 2010 from UNITED STATES Additional patient health information: Male patient , 59 years of age, . Ultram dosage: . During the same period patient was treated with AMPHETAMINES (View Amphetamines Review and Amphetamines Label ), TRICYCLIC ANTIDEPRESSANTS (View Tricyclic Antidepressants Review and Tricyclic Antidepressants Label ), ETHANOL (View Ethanol Review and Ethanol Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ).

6680960-9 | Coma, Disorientation, Dysarthria, Hypotension, Snoring
Adverse event was reported on Apr 09, 2010 by a Female patient taking Ultram (View Usage) (Dosage: ) . Location: UNITED STATES , 68 years of age, Patient experienced the following unwanted or unexpected effects: coma, disorientation, dysarthria, hypotension, snoring (What is snoring?). During the same period patient was treated with BENZODIAZEPINE NOS (View Benzodiazepine Nos Review and Benzodiazepine Nos Label ), ETHANOL (View Ethanol Review and Ethanol Label ).

6680955-5 | Loss Of Consciousness, Tachycardia
on Apr 09, 2010 Female patient from UNITED STATES , 38 years of age, was treated with Ultram (View Usage). Patient had the following side effects: loss of consciousness, tachycardia. Ultram dosage: . During the same period patient was treated with CYCLOBENZAPRINE (View Cyclobenzaprine Review and Cyclobenzaprine Label ), HUMALOG (View Humalog Review and Humalog Label ), BENZODIAZEPINE NOS (View Benzodiazepine Nos Review and Benzodiazepine Nos Label ).

6680949-X | Miosis, Oxygen Saturation Decreased, Somnolence
on Apr 09, 2010 Male patient from UNITED STATES , 36 years of age, weighting 150.0 lb, was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: miosis, oxygen saturation decreased, somnolence. Ultram dosage: . During the same period patient was treated with CYCLOBENZAPRINE (View Cyclobenzaprine Review and Cyclobenzaprine Label ), BACLOFEN (View Baclofen Review and Baclofen Label ).

6679374-7 | Aggression, Depressed Level Of Consciousness, Respiratory Depression
Patient was taking Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: aggression, depressed level of consciousness, respiratory depression on Apr 09, 2010 from UNITED STATES Additional patient health information: Male patient , 31 years of age, . Ultram dosage: . During the same period patient was treated with CYCLOBENZAPRINE (View Cyclobenzaprine Review and Cyclobenzaprine Label ), METHADONE HCL (View Methadone Hcl Review and Methadone Hcl Label ), BENZODIAZEPINE NOS (View Benzodiazepine Nos Review and Benzodiazepine Nos Label ), OPIATES (View Opiates Review and Opiates Label ), COCAINE (View Cocaine Review and Cocaine Label ), MORPHINE SULFATE (View Morphine Sulfate Review and Morphine Sulfate Label ).

6676513-9 | Acute Hepatic Failure, Confusional State
Adverse event was reported on Apr 01, 2010 by a Male patient taking Ultram (View Usage) (Dosage: ) was diagnosed with gout (What is gout?) and. Location: UNITED STATES , weighting 198.0 lb, Patient had the following side effects: acute hepatic failure, confusional state. During the same period patient was treated with ULORIC (View Uloric Review and Uloric Label ), CLONIDINE (View Clonidine Review and Clonidine Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), HYDROCODONE BITARTRATE (View Hydrocodone Bitartrate Review and Hydrocodone Bitartrate Label ), LANTUS (View Lantus Review and Lantus Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ). Patient was hospitalized.

6676057-4 | Adverse Event, Haematoma, Overdose
on Apr 05, 2010 Female patient from UNITED STATES , weighting 145.0 lb, was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: adverse event, haematoma, overdose. Ultram dosage: One Every 8-10 Hours. During the same period patient was treated with CYMBALTA (View Cymbalta Review and Cymbalta Label ), PERCOCET (View Percocet Review and Percocet Label ). Patient was hospitalized.

6672381-X | Back Disorder, Heart Rate Increased, Musculoskeletal Disorder, Sciatica, Therapeutic Response Decreased
on Mar 31, 2010 Male patient from UNITED STATES , weighting 210.0 lb, was diagnosed with neck pain, back pain (What is back pain?), arrhythmia (What is arrhythmia?) and was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: back disorder, heart rate increased, musculoskeletal disorder, sciatica (What is sciatica?), therapeutic response decreased. Ultram dosage: . During the same period patient was treated with TRAMADOL HYDROCHLORIDE (6 Times In 24 Hours As Needed) (View Tramadol Hydrochloride Review and Tramadol Hydrochloride Label ), SELOKEN ZOC (View Seloken Zoc Review and Seloken Zoc Label ). Patient was hospitalized.

6663795-2 | Abasia, Fall, Influenza Like Illness, Insomnia, Malaise, Trance
Patient was taking Ultram (View Usage). Patient had the following side effects: abasia, fall (What is fall?), influenza like illness, insomnia, malaise, trance on Mar 19, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 122.0 lb, was diagnosed with neuralgia, hypertension, respiratory disorder, nervousness and. Ultram dosage: 1 Every 6 Hours As Needed. During the same period patient was treated with TRAMADOL HCL (1 Every 6 Hours As Needed) (View Tramadol Hcl Review and Tramadol Hcl Label ), ZESTRIL (Daily) (View Zestril Review and Zestril Label ), CHLORTHALIDONE (^every Other Day^) (View Chlorthalidone Review and Chlorthalidone Label ), SPIRIVA (View Spiriva Review and Spiriva Label ), CORTISONE ACETATE (As Needed) (View Cortisone Acetate Review and Cortisone Acetate Label ), LORAZEPAM (Half Tablet Twice A Day) (View Lorazepam Review and Lorazepam Label ).

6662880-9 | Acute Hepatic Failure, Confusional State
Adverse event was reported on Mar 19, 2010 by a Male patient taking Ultram (View Usage) (Dosage: ) was diagnosed with gout (What is gout?) and. Location: UNITED STATES , weighting 198.0 lb, After Ultram was administered, patient had the following side effects: acute hepatic failure, confusional state. During the same period patient was treated with ULORIC (View Uloric Review and Uloric Label ), CLONIDINE (View Clonidine Review and Clonidine Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), HYDROCODONE (View Hydrocodone Review and Hydrocodone Label ), LANTUS (View Lantus Review and Lantus Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ). Patient was hospitalized.

6659525-0 | Fall, Influenza Like Illness
on Mar 12, 2010 Female patient from UNITED STATES , weighting 122.0 lb, was diagnosed with pain (What is pain?) and was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: fall (What is fall?), influenza like illness. Ultram dosage: 3 Times In 1 Day. During the same period patient was treated with TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ).

6645836-1 | Hallucination, Visual
on Mar 18, 2010 Male patient from UNITED STATES , 82 years of age, weighting 157.6 lb, was treated with Ultram (View Usage). Patient had the following side effects: hallucination, visual. Ultram dosage: Po.

6643626-7 | Fall, Femur Fracture
Patient was taking Ultram (View Usage). After Ultram was administered, patient had the following side effects: fall (What is fall?), femur fracture on Mar 12, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 128.0 lb, was diagnosed with fibromyalgia and. Ultram dosage: . Patient was hospitalized.

6628578-8 | Fall, Influenza Like Illness
Adverse event was reported on Mar 02, 2010 by a Female patient taking Ultram (View Usage) (Dosage: 3 Times In 1 Day) was diagnosed with pain (What is pain?) and. Location: UNITED STATES , weighting 122.0 lb, Patient experienced the following unwanted or unexpected effects: fall (What is fall?), influenza like illness. During the same period patient was treated with TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ).

6547189-6 | Blood Chloride Decreased, Hypertension, Intentional Overdose, Somnolence, Suicide Attempt, Tachypnoea
on Jan 07, 2010 Male patient from UNITED STATES , 30 years of age, weighting 180.0 lb, was diagnosed with suicide attempt and was treated with Ultram (View Usage). Patient had the following side effects: blood chloride decreased, hypertension, intentional overdose, somnolence, suicide attempt, tachypnoea. Ultram dosage: . Patient was hospitalized.

6542137-7 | Convulsion, Hypotension, Overdose, Rhabdomyolysis, Somnolence, Tachycardia, Urine Output Decreased, Vomiting
on Jan 07, 2010 Female patient from UNITED STATES , 33 years of age, was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: convulsion, hypotension, overdose, rhabdomyolysis, somnolence, tachycardia, urine output decreased, vomiting. Ultram dosage: . During the same period patient was treated with DIPHENHYDRAMINE (^taken In Large Doses All The Time^) (View Diphenhydramine Review and Diphenhydramine Label ). Patient was hospitalized.

6539835-8 | Convulsion, Overdose, Suicide Attempt, Tachycardia
Patient was taking Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion, overdose, suicide attempt, tachycardia on Jan 07, 2010 from UNITED STATES Additional patient health information: Male patient , 20 years of age, . Ultram dosage: . Patient was hospitalized.

6539638-4 | Bundle Branch Block Left, Disorientation, Dyspnoea, Sedation, Sinus Tachycardia, Unresponsive To Stimuli
Adverse event was reported on Jan 07, 2010 by a Female patient taking Ultram (View Usage) (Dosage: ) . Location: UNITED STATES , 36 years of age, Patient had the following side effects: bundle branch block left, disorientation, dyspnoea, sedation, sinus tachycardia, unresponsive to stimuli. During the same period patient was treated with ANTIPSYCHOTICS (NOS) (Dose: ^100^) (View Antipsychotics (nos) Review and Antipsychotics (nos) Label ), BENZODIAZEPINES NOS (View Benzodiazepines Nos Review and Benzodiazepines Nos Label ), TRICYCLIC ANTIDEPRESSANT (View Tricyclic Antidepressant Review and Tricyclic Antidepressant Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

6537954-3 | Angioedema
on Jan 12, 2010 Female patient from UNITED STATES , 84 years of age, weighting 175.4 lb, was diagnosed with pain (What is pain?) and was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: angioedema. Ultram dosage: 50mg (2tabs) Q 4-6h Prn Po (recent). During the same period patient was treated with IRON (View Iron Review and Iron Label ), COREG (View Coreg Review and Coreg Label ), VITAMIN K TAB (View Vitamin K Tab Review and Vitamin K Tab Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), NORCO (View Norco Review and Norco Label ), ATIVAN (View Ativan Review and Ativan Label ), SERTRALINE HCL (View Sertraline Hcl Review and Sertraline Hcl Label ). Patient was hospitalized.

6535997-7 | Blood Chloride Decreased, Hypertension, Intentional Overdose, Somnolence, Suicide Attempt, Tachypnoea
on Jan 07, 2010 Male patient from UNITED STATES , 30 years of age, weighting 180.0 lb, was diagnosed with suicide attempt and was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: blood chloride decreased, hypertension, intentional overdose, somnolence, suicide attempt, tachypnoea. Ultram dosage: . Patient was hospitalized.

6535459-7 | Angioedema, Dyspnoea, Hypersensitivity, Penis Disorder, Urticaria
Patient was taking Ultram (View Usage). Patient had the following side effects: angioedema, dyspnoea, hypersensitivity, penis disorder (What is penis disorder?), urticaria on Jan 11, 2010 from UNITED STATES Additional patient health information: Male patient , 47 years of age, weighting 205.0 lb, was diagnosed with sciatica (What is sciatica?) and. Ultram dosage: 50mg 100mg Every 4 Hrs Oral. During the same period patient was treated with GEBHARDIA (300 Mg 3x A Day Oral) (View Gebhardia Review and Gebhardia Label ).

6535381-6 | Convulsion, Laceration, Overdose, Respiratory Depression, Tachycardia
Adverse event was reported on Jan 07, 2010 by a Male patient taking Ultram (View Usage) (Dosage: ) . Location: UNITED STATES , 41 years of age, After Ultram was administered, patient had the following side effects: convulsion, laceration, overdose, respiratory depression, tachycardia. During the same period patient was treated with SSRI (View Ssri Review and Ssri Label ), ANTICONVULSANT (View Anticonvulsant Review and Anticonvulsant Label ).

6535380-4 | Unresponsive To Stimuli
on Jan 07, 2010 Male patient from UNITED STATES , 22 years of age, was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: unresponsive to stimuli. Ultram dosage: .

6535376-2 | Cardio-respiratory Arrest, Coagulation Test Abnormal, Mydriasis, Tachycardia, Unresponsive To Stimuli
on Jan 07, 2010 Male patient from UNITED STATES , 17 years of age, was treated with Ultram (View Usage). Patient had the following side effects: cardio-respiratory arrest, coagulation test abnormal, mydriasis, tachycardia, unresponsive to stimuli. Ultram dosage: . During the same period patient was treated with METHADONE (View Methadone Review and Methadone Label ), ETHANOL (View Ethanol Review and Ethanol Label ).

6535195-7 | Hypotension, Overdose, Suicide Attempt
Patient was taking Ultram (View Usage). After Ultram was administered, patient had the following side effects: hypotension, overdose, suicide attempt on Jan 07, 2010 from UNITED STATES Additional patient health information: Male patient , 41 years of age, . Ultram dosage: . During the same period patient was treated with ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), CLONIDINE (View Clonidine Review and Clonidine Label ), PHENYTOIN (View Phenytoin Review and Phenytoin Label ).

6535190-8 | Apnoea, Atrioventricular Block First Degree, Bundle Branch Block, Electrocardiogram St Segment Depression, Intentional Overdose, Somnolence, Speech Disorder
Adverse event was reported on Jan 07, 2010 by a Female patient taking Ultram (View Usage) (Dosage: ) . Location: UNITED STATES , 78 years of age, Patient experienced the following unwanted or unexpected effects: apnoea, atrioventricular block first degree, bundle branch block, electrocardiogram st segment depression, intentional overdose, somnolence, speech disorder. During the same period patient was treated with AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ), BENZODIAZEPINE NOS (View Benzodiazepine Nos Review and Benzodiazepine Nos Label ).

6534556-X | Apnoea, Depressed Level Of Consciousness, Hypertension, Overdose
on Jan 07, 2010 Male patient from UNITED STATES , 22 years of age, was diagnosed with joint injury and was treated with Ultram (View Usage). Patient had the following side effects: apnoea, depressed level of consciousness, hypertension, overdose. Ultram dosage: . During the same period patient was treated with NSAID (View Nsaid Review and Nsaid Label ), ANTICONVULSANT (View Anticonvulsant Review and Anticonvulsant Label ), MELOXICAM (View Meloxicam Review and Meloxicam Label ).

6533531-9 | Electrocardiogram Qt Prolonged, Grand Mal Convulsion, Suicide Attempt, Supraventricular Extrasystoles, Tachycardia
on Jan 07, 2010 Female patient from UNITED STATES , 32 years of age, was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: electrocardiogram qt prolonged, grand mal convulsion, suicide attempt, supraventricular extrasystoles, tachycardia. Ultram dosage: . During the same period patient was treated with TIZANIDINE HCL (View Tizanidine Hcl Review and Tizanidine Hcl Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ), MUSCLE RELAXANTS (NOS) (View Muscle Relaxants (nos) Review and Muscle Relaxants (nos) Label ), ANTICONVULSANT (View Anticonvulsant Review and Anticonvulsant Label ).

6533529-0 | Unresponsive To Stimuli
Patient was taking Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: unresponsive to stimuli on Jan 07, 2010 from UNITED STATES Additional patient health information: Female patient , 50 years of age, . Ultram dosage: . During the same period patient was treated with CARISOPRODOL (View Carisoprodol Review and Carisoprodol Label ), BUPRENORPHINE (View Buprenorphine Review and Buprenorphine Label ), ANTIHISTAMINES (View Antihistamines Review and Antihistamines Label ), BENZODIAZEPINE NOS (View Benzodiazepine Nos Review and Benzodiazepine Nos Label ).

6501509-7 | Abdominal Pain Upper, Decreased Appetite, Feeling Abnormal, Gastrointestinal Pain, Malaise, Nightmare, Suicidal Ideation, Withdrawal Syndrome
Adverse event was reported on Dec 15, 2009 by a Male patient taking Ultram (View Usage) (Dosage: 1 Pill Daily Po) . Location: UNITED STATES , weighting 198.0 lb, Patient had the following side effects: abdominal pain upper, decreased appetite, feeling abnormal, gastrointestinal pain, malaise, nightmare, suicidal ideation, withdrawal syndrome. Patient was hospitalized.

6490883-6 | Blood Creatine Phosphokinase Increased, Convulsion, Hypertension, Hypotension, Unresponsive To Stimuli
on Oct 21, 2008 Male patient from UNITED STATES , 27 years of age, was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: blood creatine phosphokinase increased, convulsion, hypertension, hypotension, unresponsive to stimuli. Ultram dosage: . During the same period patient was treated with MUSCLE RELAXANT (View Muscle Relaxant Review and Muscle Relaxant Label ), ANTICONVULSANT (View Anticonvulsant Review and Anticonvulsant Label ), DULOXETINE HYDROCHLORIDE (View Duloxetine Hydrochloride Review and Duloxetine Hydrochloride Label ), KADIAN (View Kadian Review and Kadian Label ), OXYCODONE (View Oxycodone Review and Oxycodone Label ), PHENCYCLIDINE (View Phencyclidine Review and Phencyclidine Label ). Patient was hospitalized.

6468458-4 | Confusional State, Screaming, Tremor
on Dec 02, 2009 Female patient from UNITED STATES , 93 years of age, was diagnosed with pain (What is pain?) and was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: confusional state, screaming, tremor. Ultram dosage: 50mg Po.

6426090-2 | Dizziness, Dyspnoea, Hallucination, Nausea, Palpitations, Paraesthesia, Pruritus, Somnolence
Patient was taking Ultram (View Usage). Patient had the following side effects: dizziness (What is dizziness?), dyspnoea, hallucination, nausea (What is nausea?), palpitations, paraesthesia, pruritus, somnolence on Nov 03, 2009 from UNITED STATES Additional patient health information: Female patient , 45 years of age, weighting 147.0 lb, was diagnosed with back pain (What is back pain?) and. Ultram dosage: 50mg Once Oral 047 One Pill.

6411998-4 | Aspartate Aminotransferase Increased, Coma
Adverse event was reported on Oct 14, 2009 by a Male patient taking Ultram (View Usage) (Dosage: ) . Location: UNITED STATES , 46 years of age, After Ultram was administered, patient had the following side effects: aspartate aminotransferase increased, coma. During the same period patient was treated with ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), CYCLOBENZAPRINE (View Cyclobenzaprine Review and Cyclobenzaprine Label ), METHADONE HYDROCHLORIDE (View Methadone Hydrochloride Review and Methadone Hydrochloride Label ), MARIJUANA (View Marijuana Review and Marijuana Label ), METHAMPHETAMINE (View Methamphetamine Review and Methamphetamine Label ), AMPHETAMINE SULFATE (View Amphetamine Sulfate Review and Amphetamine Sulfate Label ), TRICYCLIC ANTIDEPRESSANT (View Tricyclic Antidepressant Review and Tricyclic Antidepressant Label ).

6411587-1 | Hypotension, Loss Of Consciousness, Overdose, Suicide Attempt
on Oct 14, 2009 Female patient from UNITED STATES , 57 years of age, was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: hypotension, loss of consciousness, overdose, suicide attempt. Ultram dosage: . During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), TRICYCLIC ANTIDEPRESSANT (View Tricyclic Antidepressant Review and Tricyclic Antidepressant Label ), BARBITURATES (View Barbiturates Review and Barbiturates Label ).

6411585-8 | Convulsion, Foaming At Mouth, Hypertension, Mydriasis, Overdose, Tachycardia, Unresponsive To Stimuli
on Oct 14, 2009 Male patient from UNITED STATES , 23 years of age, was treated with Ultram (View Usage). Patient had the following side effects: convulsion, foaming at mouth, hypertension, mydriasis, overdose, tachycardia, unresponsive to stimuli. Ultram dosage: . During the same period patient was treated with VICODIN ES (View Vicodin Es Review and Vicodin Es Label ). Patient was hospitalized.

6411584-6 | Convulsion, Hypertension
Patient was taking Ultram (View Usage). After Ultram was administered, patient had the following side effects: convulsion, hypertension on Oct 14, 2009 from UNITED STATES Additional patient health information: Female patient , 35 years of age, . Ultram dosage: . Patient was hospitalized.

6411583-4 | Convulsion, Overdose, Ventricular Tachycardia
Adverse event was reported on Oct 14, 2009 by a Female patient taking Ultram (View Usage) (Dosage: ) . Location: UNITED STATES , 75 years of age, Patient experienced the following unwanted or unexpected effects: convulsion, overdose, ventricular tachycardia. Patient was hospitalized.

6411582-2 | Convulsion, Overdose
on Oct 14, 2009 Male patient from UNITED STATES , 28 years of age, was diagnosed with arthralgia and was treated with Ultram (View Usage). Patient had the following side effects: convulsion, overdose. Ultram dosage: Dose: 5-6. During the same period patient was treated with ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

6404179-1 | Chest Discomfort, Dysphagia, Dyspnoea
on Oct 05, 2009 Female patient from UNITED STATES , weighting 200.0 lb, was diagnosed with back pain (What is back pain?), cardiac disorder, blood cholesterol increased and was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: chest discomfort, dysphagia, dyspnoea. Ultram dosage: Stop Date: 2009. During the same period patient was treated with TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), COZAAR (View Cozaar Review and Cozaar Label ), LIPITOR (View Lipitor Review and Lipitor Label ), NAPROXEN (View Naproxen Review and Naproxen Label ).

6383658-X | Feeling Abnormal, Impaired Driving Ability
Patient was taking Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: feeling abnormal, impaired driving ability on Sep 29, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 170.0 lb, was diagnosed with pain (What is pain?) and. Ultram dosage: 200 Mg Daily Po.

6376474-6 | Dizziness, Fatigue, Feeling Abnormal, Nausea, Presyncope
Adverse event was reported on Sep 22, 2009 by a Female patient taking Ultram (View Usage) (Dosage: 200mg Daily Po) was diagnosed with back pain (What is back pain?) and. Location: UNITED STATES , 41 years of age, weighting 149.0 lb, Patient had the following side effects: dizziness (What is dizziness?), fatigue, feeling abnormal, nausea (What is nausea?), presyncope.

6315079-X | Convulsion, Dizziness, Head Injury, Loss Of Consciousness
on Aug 18, 2009 Female patient from UNITED STATES , 26 years of age, weighting 124.0 lb, was diagnosed with back pain (What is back pain?) and was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: convulsion, dizziness (What is dizziness?), head injury, loss of consciousness. Ultram dosage: One By Mouth 2x Day Everyday. Patient was hospitalized.

6309615-7 | Abdominal Discomfort, Inadequate Analgesia, Insomnia, Pathological Fracture
on Jul 31, 2009 Female patient from UNITED STATES , weighting 117.0 lb, was diagnosed with osteoporosis (What is osteoporosis?) and was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal discomfort, inadequate analgesia, insomnia, pathological fracture. Ultram dosage: 2x 50 Mg, Every 4-6 Hours. Patient was hospitalized.

6303934-6 | Coma, Hallucination, Lethargy, Refusal Of Treatment By Relative, Somnolence
Patient was taking Ultram (View Usage). Patient had the following side effects: coma, hallucination, lethargy, refusal of treatment by relative, somnolence on Aug 10, 2009 from UNITED STATES Additional patient health information: Male patient , 68 years of age, weighting 170.0 lb, was diagnosed with pain (What is pain?) and. Ultram dosage: 50 Mg. 5 Times Daily.

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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 Ultram 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 Ultram quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Ultram 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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Ultram Reactions
Asthenia
Chest PainWhat is Chest pain?
Coma
Confusional State
Convulsion
Depressed Level Of Consciousness
Diarrhoea
DizzinessWhat is Dizziness?
Dyspnoea
FallWhat is Fall?
Feeling Abnormal
Grand Mal Convulsion
HeadacheWhat is Headache?
Hypertension
Hypotension
Insomnia
Lethargy
Loss Of Consciousness
Myocardial Infarction
NauseaWhat is Nausea?
Overdose
Respiratory Depression
Somnolence
Suicidal Ideation
Suicide Attempt
Tachycardia
Tremor
Unresponsive To Stimuli
Vomiting
Withdrawal Syndrome
Ultram 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 Ultram 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!