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Summary

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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6985681-0 | Coma, Hypoxia
on Sep 13, 2010 Female patient from UNITED STATES , weighting 155.0 lb, was diagnosed with arthralgia, thyroid disorder, migraine (What is migraine?) and was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: coma, hypoxia. Ultram dosage: Stopped In Oct-2009. During the same period patient was treated with SYNTHROID (View Synthroid Review and Synthroid Label ), AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ). Patient was hospitalized.

6940777-4 | Contraindication To Medical Treatment, Insomnia, Myocardial Infarction, Tachycardia
Patient was taking Ultram (View Usage). Patient had the following side effects: contraindication to medical treatment, insomnia, myocardial infarction, tachycardia on Aug 16, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 130.0 lb, was diagnosed with complex regional pain syndrome (What is complex regional pain syndrome?) and. Ultram dosage: . During the same period patient was treated with NEURONTIN (View Neurontin Review and Neurontin Label ), LORTAB (View Lortab Review and Lortab Label ). Patient was hospitalized.

6929569-X | Cardiac Arrest, Disturbance In Social Behaviour, Overdose, Suicidal Ideation, Suicide Attempt, Treatment Noncompliance
Adverse event was reported on Aug 16, 2010 by a Female patient taking Ultram (View Usage) (Dosage: ) was diagnosed with musculoskeletal pain, injury and. Location: UNITED STATES , weighting 138.0 lb, After Ultram was administered, patient had the following side effects: cardiac arrest (What is cardiac arrest?), disturbance in social behaviour, overdose, suicidal ideation, suicide attempt, treatment noncompliance. Patient was hospitalized.

6923760-4 | Myocardial Infarction
on Aug 06, 2010 Male patient from UNITED STATES , weighting 206.0 lb, was diagnosed with back pain (What is back pain?), blood pressure (What is blood pressure?) and was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: myocardial infarction. Ultram dosage: Two 50 Mg Tablets Every 4-6 Hours. During the same period patient was treated with LISINOPRIL (20 Mg Once A Day) (View Lisinopril Review and Lisinopril Label ), LORTAB (7.5/500 Mg Tablet/ 4 Times In 24 Hours) (View Lortab Review and Lortab Label ).


6914601-X | Lip Swelling, Swelling Face
on Aug 04, 2010 Female patient from UNITED STATES , 84 years of age, was diagnosed with arthralgia and was treated with Ultram (View Usage). Patient had the following side effects: lip swelling, swelling face. Ultram dosage: 50mg Bid Oral (po). Patient was hospitalized.

6911414-X | Coma, Hypoxia
Patient was taking Ultram (View Usage). After Ultram was administered, patient had the following side effects: coma, hypoxia on Jul 29, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 155.0 lb, was diagnosed with arthralgia, thyroid disorder, migraine (What is migraine?) and. Ultram dosage: Stopped In Oct-2009. During the same period patient was treated with SYNTHROID (View Synthroid Review and Synthroid Label ), AMITRIPTYLINE HYDROCHLORIDE (View Amitriptyline Hydrochloride Review and Amitriptyline Hydrochloride Label ). Patient was hospitalized.

6888215-4 | Cardiac Arrest, Disturbance In Social Behaviour, Overdose, Suicidal Ideation, Suicide Attempt, Treatment Noncompliance
Adverse event was reported on Jul 26, 2010 by a Female patient taking Ultram (View Usage) (Dosage: ) was diagnosed with musculoskeletal pain, injury and. Location: UNITED STATES , weighting 138.0 lb, Patient experienced the following unwanted or unexpected effects: cardiac arrest (What is cardiac arrest?), disturbance in social behaviour, overdose, suicidal ideation, suicide attempt, treatment noncompliance. Patient was hospitalized.

6887154-2 | Adverse Event, Haematoma, Overdose, Withdrawal Syndrome
on Jul 21, 2010 Female patient from UNITED STATES , weighting 145.0 lb, was diagnosed with pain (What is pain?) and was treated with Ultram (View Usage). Patient had the following side effects: adverse event, haematoma, overdose, withdrawal syndrome. 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.

6882777-9 | Contraindication To Medical Treatment, Insomnia, Myocardial Infarction, Tachycardia
on Jul 20, 2010 Female patient from UNITED STATES , weighting 130.0 lb, was diagnosed with complex regional pain syndrome (What is complex regional pain syndrome?) and was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: contraindication to medical treatment, insomnia, myocardial infarction, tachycardia. Ultram dosage: . During the same period patient was treated with NEURONTIN (View Neurontin Review and Neurontin Label ), LORTAB (View Lortab Review and Lortab Label ). Patient was hospitalized.

6882224-7 | Myocardial Infarction
Patient was taking Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: myocardial infarction on Jul 19, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 206.0 lb, was diagnosed with back pain (What is back pain?), blood pressure (What is blood pressure?) and. Ultram dosage: Two 50 Mg Tablets Every 4-6 Hours. During the same period patient was treated with LISINOPRIL (20 Mg Once A Day) (View Lisinopril Review and Lisinopril Label ), LORTAB (7.5/500 Mg Tablet/ 4 Times In 24 Hours) (View Lortab Review and Lortab Label ).

6881431-7 | Completed Suicide, Gun Shot Wound
Adverse event was reported on Jul 28, 2010 by a Male patient taking Ultram (View Usage) (Dosage: 50mg Every 8 Hours Po) was diagnosed with radiculopathy and. Location: UNITED STATES , weighting 287.0 lb, Patient had the following side effects: completed suicide, gun shot wound.

6871916-1 | Confusional State, Loss Of Consciousness, Respiratory Arrest
on Jul 21, 2010 Female patient from UNITED STATES , 91 years of age, was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: confusional state, loss of consciousness, respiratory arrest. Ultram dosage: . During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ).

6866435-2 | Lethargy, Self Injurious Behaviour, Vomiting
on Jul 12, 2010 Female patient from UNITED STATES , 28 years of age, was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: lethargy, self injurious behaviour, vomiting. Ultram dosage: . During the same period patient was treated with ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), CYCLOBENZAPRINE (View Cyclobenzaprine Review and Cyclobenzaprine Label ), BENZODIAZEPINE NOS (View Benzodiazepine Nos Review and Benzodiazepine Nos Label ), ETHANOL (View Ethanol Review and Ethanol Label ), PROPRANOLOL (View Propranolol Review and Propranolol Label ), TRAZODONE (View Trazodone Review and Trazodone Label ), HYDROCODONE BITARTRATE (View Hydrocodone Bitartrate Review and Hydrocodone Bitartrate Label ). Patient was hospitalized.

6866434-0 | Loss Of Consciousness, Pulse Absent
Patient was taking Ultram (View Usage). Patient had the following side effects: loss of consciousness, pulse absent on Jul 15, 2010 from UNITED STATES Additional patient health information: Female patient , 20 years of age, . Ultram dosage: . During the same period patient was treated with CYCLOBENZAPRINE (View Cyclobenzaprine Review and Cyclobenzaprine Label ), MUSCLE RELAXANTS (View Muscle Relaxants Review and Muscle Relaxants Label ), ACETAMINOPHEN W/ PROPOXYPHENE HCL (View Acetaminophen W/ Propoxyphene Hcl Review and Acetaminophen W/ Propoxyphene Hcl Label ). Patient was hospitalized.

6866410-8 | Confusional State, Loss Of Consciousness, Respiratory Arrest
Adverse event was reported on Jul 13, 2010 by a Female patient taking Ultram (View Usage) (Dosage: ) . Location: UNITED STATES , 91 years of age, After Ultram was administered, patient had the following side effects: confusional state, loss of consciousness, respiratory arrest. During the same period patient was treated with FENTANYL (View Fentanyl Review and Fentanyl Label ).

6866407-8 | Abdominal Tenderness, Hypotension, Overdose, Oxygen Saturation Decreased
on Jul 13, 2010 Female patient from UNITED STATES , 52 years of age, was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal tenderness, hypotension, overdose, oxygen saturation decreased. Ultram dosage: . During the same period patient was treated with ACE INHIBITOR (View Ace Inhibitor Review and Ace Inhibitor Label ), CALCIUM ANTAGONISTS (View Calcium Antagonists Review and Calcium Antagonists Label ), PROGESTIN INJ (View Progestin Inj Review and Progestin Inj Label ), ANTICONVULSANT (View Anticonvulsant Review and Anticonvulsant Label ), THYROID PREPARATIONS (View Thyroid Preparations Review and Thyroid Preparations Label ), LOTENSIN (View Lotensin Review and Lotensin Label ), BUPROPION (View Bupropion Review and Bupropion Label ), PROTON PUMP INHIBITOR (View Proton Pump Inhibitor Review and Proton Pump Inhibitor Label ).

6866406-6 | Hypotension, Tachycardia
on Jul 13, 2010 Male patient from UNITED STATES , 52 years of age, was treated with Ultram (View Usage). Patient had the following side effects: hypotension, tachycardia. Ultram dosage: . During the same period patient was treated with BENZODIAZEPINE NOS (View Benzodiazepine Nos Review and Benzodiazepine Nos Label ), ANTIPSYCHOTIC (100 Mg And 300 Mg, 3 Per Day) (View Antipsychotic Review and Antipsychotic Label ), METFORMIN (View Metformin Review and Metformin Label ), THIAZOLIDINEDIONE (View Thiazolidinedione Review and Thiazolidinedione Label ), TERAZOSIN HCL (View Terazosin Hcl Review and Terazosin Hcl Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), RANITIDINE (View Ranitidine Review and Ranitidine Label ).

6861200-4 | Gastrooesophageal Reflux Disease, Hand Fracture, Joint Injury, Pain, Rotator Cuff Syndrome, Suicidal Ideation
Patient was taking Ultram (View Usage). After Ultram was administered, patient had the following side effects: gastrooesophageal reflux disease, hand fracture, joint injury, pain (What is pain?), rotator cuff syndrome, suicidal ideation on Jul 09, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 160.0 lb, was diagnosed with pain (What is pain?) and. Ultram dosage: As Needed. During the same period patient was treated with TRAMADOL (As Needed) (View Tramadol Review and Tramadol Label ).

6843753-5 | Gastrooesophageal Reflux Disease, Hand Fracture, Joint Injury, Pain, Rotator Cuff Syndrome, Suicidal Ideation
Adverse event was reported on Jul 13, 2010 by a Female patient taking Ultram (View Usage) (Dosage: As Needed) was diagnosed with pain (What is pain?) and. Location: UNITED STATES , weighting 160.0 lb, Patient experienced the following unwanted or unexpected effects: gastrooesophageal reflux disease, hand fracture, joint injury, pain (What is pain?), rotator cuff syndrome, suicidal ideation. During the same period patient was treated with TRAMADOL HCL (As Needed) (View Tramadol Hcl Review and Tramadol Hcl Label ).

6839365-X | Loss Of Consciousness, Pulse Absent
on Jul 07, 2010 Female patient from UNITED STATES , 20 years of age, was treated with Ultram (View Usage). Patient had the following side effects: loss of consciousness, pulse absent. Ultram dosage: . During the same period patient was treated with CYCLOBENZAPRINE (View Cyclobenzaprine Review and Cyclobenzaprine Label ), MUSCLE RELAXANTS (View Muscle Relaxants Review and Muscle Relaxants Label ), ACETAMINOPHEN W/ PROPOXYPHENE HCL (View Acetaminophen W/ Propoxyphene Hcl Review and Acetaminophen W/ Propoxyphene Hcl Label ). Patient was hospitalized.

6835689-0 | Confusional State, Loss Of Consciousness, Respiratory Arrest
on Jul 07, 2010 Female patient from UNITED STATES , 91 years of age, was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: confusional state, loss of consciousness, respiratory arrest. Ultram dosage: . During the same period patient was treated with FENTANYL CITRATE (View Fentanyl Citrate Review and Fentanyl Citrate Label ).

6835687-7 | Abdominal Tenderness, Hypotension, Overdose, Oxygen Saturation Decreased
Patient was taking Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal tenderness, hypotension, overdose, oxygen saturation decreased on Jul 07, 2010 from UNITED STATES Additional patient health information: Female patient , 52 years of age, . Ultram dosage: . During the same period patient was treated with ACE INHIBITOR (View Ace Inhibitor Review and Ace Inhibitor Label ), CALCIUM ANTAGONISTS (View Calcium Antagonists Review and Calcium Antagonists Label ), PROGESTIN INJ (View Progestin Inj Review and Progestin Inj Label ), ANTICONVULSANT (View Anticonvulsant Review and Anticonvulsant Label ), THYROID PREPARATIONS (View Thyroid Preparations Review and Thyroid Preparations Label ), LOTENSIN (View Lotensin Review and Lotensin Label ), BUPROPION (View Bupropion Review and Bupropion Label ), PROTON PUMP INHIBITOR (View Proton Pump Inhibitor Review and Proton Pump Inhibitor Label ).

6835653-1 | Lethargy, Self Injurious Behaviour, Vomiting
Adverse event was reported on Jul 07, 2010 by a Female patient taking Ultram (View Usage) (Dosage: ) . Location: UNITED STATES , 28 years of age, Patient had the following side effects: lethargy, self injurious behaviour, vomiting. During the same period patient was treated with ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), CYCLOBENZAPRINE (View Cyclobenzaprine Review and Cyclobenzaprine Label ), BENZODIAZEPINE NOS (View Benzodiazepine Nos Review and Benzodiazepine Nos Label ), ETHANOL (View Ethanol Review and Ethanol Label ), PROPRANOLOL (View Propranolol Review and Propranolol Label ), TRAZODONE HYDROCHLORIDE (View Trazodone Hydrochloride Review and Trazodone Hydrochloride Label ), HYDROCODONE BITARTRATE (View Hydrocodone Bitartrate Review and Hydrocodone Bitartrate Label ). Patient was hospitalized.

6835648-8 | Hypotension, Tachycardia
on Jul 07, 2010 Male patient from UNITED STATES , 52 years of age, was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: hypotension, tachycardia. Ultram dosage: . During the same period patient was treated with BENZODIAZEPINE NOS (View Benzodiazepine Nos Review and Benzodiazepine Nos Label ), ANTIPSYCHOTIC (100 Mg And 300 Mg, 3 Per Day) (View Antipsychotic Review and Antipsychotic Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), THIAZOLIDINEDIONE (View Thiazolidinedione Review and Thiazolidinedione Label ), TERAZOSIN HCL (View Terazosin Hcl Review and Terazosin Hcl Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), RANITIDINE (View Ranitidine Review and Ranitidine Label ).

6826447-1 | Diplegia
on Jul 01, 2010 Female patient from UNITED STATES , 44 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: diplegia. Ultram dosage: As Needed.

6820288-7 | Abasia, Asthenia, Bedridden, Cough, Foreign Body, Gastrooesophageal Reflux Disease, Hand Fracture, Headache, Hyperhidrosis
Patient was taking Ultram (View Usage). Patient had the following side effects: abasia, asthenia, bedridden, cough, foreign body, gastrooesophageal reflux disease, hand fracture, headache (What is headache?), hyperhidrosis on Jun 30, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 160.0 lb, was diagnosed with pain (What is pain?) and. Ultram dosage: As Needed. During the same period patient was treated with TRAMADOL (As Needed) (View Tramadol Review and Tramadol Label ), ULTRAM ER (Extended Release, 2 Times A Day) (View Ultram Er Review and Ultram Er Label ).

6810446-X | Coma, Disorientation, Dysarthria, Hypotension, Snoring
Adverse event was reported on Jun 22, 2010 by a Female patient taking Ultram (View Usage) (Dosage: ) . Location: UNITED STATES , 68 years of age, After Ultram was administered, patient had the following side 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 ).

6802944-X | Poisoning, Unresponsive To Stimuli
on Jun 22, 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 ).

6802916-5 | Hypertension, Miosis, Overdose, Somnolence, Unresponsive To Stimuli
on Jun 22, 2010 Female patient from UNITED STATES , 43 years of age, was treated with Ultram (View Usage). Patient had the following side effects: hypertension, miosis, overdose, somnolence, unresponsive to stimuli. Ultram dosage: . During the same period patient was treated with AMITRIPTYLINE (View Amitriptyline Review and Amitriptyline Label ), BENZODIAZEPINE NOS (View Benzodiazepine Nos Review and Benzodiazepine Nos Label ).

6796019-6 | Back Pain, Body Height Decreased, Chest Pain, Dizziness, Dysstasia, Gastrooesophageal Reflux Disease, Headache, Muscle Spasms, Muscle Twitching
Patient was taking Ultram (View Usage). After Ultram was administered, patient had the following side effects: back pain (What is back pain?), body height decreased, chest pain (What is chest pain?), dizziness (What is dizziness?), dysstasia, gastrooesophageal reflux disease, headache (What is headache?), muscle spasms, muscle twitching on Jun 18, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 190.0 lb, was diagnosed with back pain (What is back pain?) and. Ultram dosage: Three Times A Day.

6781502-X | Dyspnoea, Erythema, Oedema Peripheral, Rash
Adverse event was reported on Jun 17, 2010 by a Female patient taking Ultram (View Usage) (Dosage: Q6 Prn 6/4/10 Qa (only Dose)) was diagnosed with fibromyalgia, headache (What is headache?) and. Location: UNITED STATES , 33 years of age, weighting 208.0 lb, Patient experienced the following unwanted or unexpected effects: dyspnoea, erythema, oedema peripheral, rash (What is rash?).

6773911-X | Product Substitution Issue
on Jun 15, 2010 Female patient from UNITED STATES , weighting 249.0 lb, was diagnosed with back pain (What is back pain?), diabetes mellitus, fibromyalgia, neuropathy peripheral and was treated with Ultram (View Usage). Patient had the following side effects: product substitution issue. Ultram dosage: 50 Mg - 100 Mg Every 4 Hr Orally. During the same period patient was treated with NEURONTIN (900 Mg Qd @ Hs Orally) (View Neurontin Review and Neurontin Label ).

6767188-9 | Adverse Event, Haematoma, Overdose, Withdrawal Syndrome
on Jun 07, 2010 Female patient from UNITED STATES , weighting 145.0 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: adverse event, haematoma, overdose, withdrawal syndrome. 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.

6762497-1 | Coma, Convulsion, Hypertension, Lethargy, Miosis, Respiratory Depression, Sedation, Suicide Attempt
Patient was taking Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: coma, convulsion, hypertension, lethargy, miosis, respiratory depression, sedation, suicide attempt on Jun 04, 2010 from UNITED STATES Additional patient health information: Female patient , 30 years of age, . Ultram dosage: . During the same period patient was treated with BENZODIAZEPINES NOS (View Benzodiazepines Nos Review and Benzodiazepines Nos Label ).

6753494-0 | Convulsion, Hypotension, Overdose, Rhabdomyolysis, Somnolence, Tachycardia, Urine Output Decreased, Vomiting
Adverse event was reported on Jun 01, 2010 by a Female patient taking Ultram (View Usage) (Dosage: ) . Location: UNITED STATES , 33 years of age, Patient had the following side effects: convulsion, hypotension, overdose, rhabdomyolysis, somnolence, tachycardia, urine output decreased, vomiting. During the same period patient was treated with DIPHENHYDRAMINE HCL (^taken In Large Doses All The Time^) (View Diphenhydramine Hcl Review and Diphenhydramine Hcl Label ). Patient was hospitalized.

6753031-0 | Electrocardiogram Qt Prolonged, Overdose, Somnolence, Vomiting
on Jun 01, 2010 Female patient from UNITED STATES , 47 years of age, was diagnosed with pain (What is pain?) and was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: electrocardiogram qt prolonged, overdose, somnolence, vomiting. Ultram dosage: . During the same period patient was treated with ANTICONVULSANT (View Anticonvulsant Review and Anticonvulsant Label ). Patient was hospitalized.

6749863-5 | Diplegia
on May 24, 2010 Female patient from UNITED STATES , 44 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: diplegia. Ultram dosage: As Needed.

6724856-2 | Product Label Confusion
Patient was taking Ultram (View Usage). Patient had the following side effects: product label confusion on May 13, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 255.5 lb, was diagnosed with spinal column injury and. Ultram dosage: 50 Mg Total Of 600 Mg A Day Oral.

6717062-9 | Fall, Femur Fracture, Weight Decreased
Adverse event was reported on May 03, 2010 by a Female patient taking Ultram (View Usage) (Dosage: ) was diagnosed with fibromyalgia, blood pressure (What is blood pressure?) and. Location: UNITED STATES , weighting 126.0 lb, After Ultram was administered, patient had the following side effects: fall (What is fall?), femur fracture, weight decreased. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ). Patient was hospitalized.

6691873-0 | Unresponsive To Stimuli
on Apr 20, 2010 Male patient from UNITED STATES , 59 years of age, was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: unresponsive to stimuli. 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 ).

6691584-1 |
on Apr 12, 2010 Female patient from UNITED STATES , weighting 132.3 lb, was diagnosed with back pain (What is back pain?) and was treated with Ultram (View Usage). . Ultram dosage: 8 Tablets Taken. During the same period patient was treated with VALIUM (2-5mg) (View Valium Review and Valium Label ).

6688898-8 | Back Pain, Body Height Decreased, Chest Pain, Dizziness, Dysstasia, Gastrooesophageal Reflux Disease, Headache, Muscle Spasms, Muscle Twitching
Patient was taking Ultram (View Usage). After Ultram was administered, patient had the following side effects: back pain (What is back pain?), body height decreased, chest pain (What is chest pain?), dizziness (What is dizziness?), dysstasia, gastrooesophageal reflux disease, headache (What is headache?), muscle spasms, muscle twitching on Apr 12, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 190.0 lb, was diagnosed with back pain (What is back pain?) and. Ultram dosage: Three Times A Day.

6688232-3 | Dependence, Haematoma, Overdose, Withdrawal Syndrome
Adverse event was reported on Apr 19, 2010 by a Female patient taking Ultram (View Usage) (Dosage: 1 Tablet Every 8-10 Hours) . Location: UNITED STATES , 47 years of age, weighting 145.0 lb, Patient experienced the following unwanted or unexpected effects: dependence, haematoma, overdose, withdrawal syndrome. 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.

6688231-1 | Adverse Event, Haematoma, Overdose, Withdrawal Syndrome
on Apr 19, 2010 Female patient from UNITED STATES , weighting 145.0 lb, was treated with Ultram (View Usage). Patient had the following side effects: adverse event, haematoma, overdose, withdrawal syndrome. 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.

6686088-6 | Convulsion, Somnolence, Tachycardia
on Apr 09, 2010 Female patient from UNITED STATES , 35 years of age, was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: convulsion, somnolence, tachycardia. Ultram dosage: 10 Tablets. During the same period patient was treated with ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

6684745-9 | Dependence, Haematoma, Overdose, Withdrawal Syndrome
Patient was taking Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: dependence, haematoma, overdose, withdrawal syndrome on Apr 05, 2010 from UNITED STATES Additional patient health information: Female patient , 47 years of age, weighting 145.0 lb, . Ultram dosage: 1 Tablet 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.

6684378-4 | Blood Potassium Decreased, Convulsion, Overdose
Adverse event was reported on Apr 09, 2010 by a Male patient taking Ultram (View Usage) (Dosage: ) . Location: UNITED STATES , 45 years of age, Patient had the following side effects: blood potassium decreased, convulsion, overdose. During the same period patient was treated with ETHANOL (View Ethanol Review and Ethanol Label ).

6684272-9 | Abnormal Behaviour, Agitation, Atrial Fibrillation, Blood Potassium Decreased, Confusional State, Loss Of Consciousness, Tachycardia
on Apr 09, 2010 Female patient from UNITED STATES , 51 years of age, was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: abnormal behaviour, agitation, atrial fibrillation (What is atrial fibrillation?), blood potassium decreased, confusional state, loss of consciousness, tachycardia. Ultram dosage: . During the same period patient was treated with DULOXETINE HYDROCHLORIDE (View Duloxetine Hydrochloride Review and Duloxetine Hydrochloride Label ), BENZODIAZEPINE NOS (View Benzodiazepine Nos Review and Benzodiazepine Nos Label ). Patient was hospitalized.

6681292-5 | Hypertension, Miosis, Overdose, Unresponsive To Stimuli
on Apr 09, 2010 Female patient from UNITED STATES , 43 years of age, was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: hypertension, miosis, overdose, unresponsive to stimuli. Ultram dosage: . During the same period patient was treated with AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), BENZODIAZEPINE NOS (View Benzodiazepine Nos Review and Benzodiazepine Nos Label ).

6681036-7 | Overdose, Suicidal Behaviour, Unresponsive To Stimuli
Patient was taking Ultram (View Usage). Patient had the following side effects: overdose, suicidal behaviour, unresponsive to stimuli on Apr 09, 2010 from UNITED STATES Additional patient health information: Female patient , 29 years of age, . Ultram dosage: . During the same period patient was treated with CYCLOBENZAPRINE (Total Dose Was Reported As 64mg) (View Cyclobenzaprine Review and Cyclobenzaprine Label ), BENZODIAZEPINE NOS (View Benzodiazepine Nos Review and Benzodiazepine Nos Label ), OXYCODONE HCL AND ACETAMINOPHEN (View Oxycodone Hcl And Acetaminophen Review and Oxycodone Hcl And Acetaminophen Label ).

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

Be aware of the following potential 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!