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Index of reports
> Cases resulting in hospitalization (14)
Below is the selection of adverse event reports related to Ultram (Tramadol) that includes cases resulting in hospitalization.
Adverse event in female receiving Ultram (Tramadol)
Reported by a consumer/non-health professional from United States on 2007-10-25
Patient: female
Adverse reactions / side effects: Weight Increased, Drug Administered AT Inappropriate Site, Inappropriate Schedule of Drug Administration, Wrong Technique in Drug Usage Process, Neck Pain, Pain in Extremity, Peripheral Vascular Disorder, Depression, Pharmaceutical Product Complaint, Cardiac Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Duragesic-100
Dosage: 12.5 ug/hr and 100 ug/hr
Indication: Pain
Ultram
Administration route: Oral
Indication: Pain
Other drugs received by patient: Percocet; Vicodin; Benadryl; Neurontin
Adverse event in 3 month old male receiving Ultram (Tramadol)
Reported by a physician from United States on 2007-10-19
Patient: 3 month old male, weighing 6.6 kg (14.5 pounds)
Adverse reactions / side effects: Overdose, Stridor, Respiratory Failure, Depressed Level of Consciousness, Drug Administration Error
Adverse event resulted in: hospitalization
Suspect drug(s):
Ultram (Tramadol)
Adverse event in 57 year old female receiving Ultram (Tramadol)
Reported by a lawyer from United States on 2007-06-21
Patient: 57 year old female
Adverse reactions / side effects: Respiratory Failure, Pneumonia Streptococcal, Mitral Valve Incompetence, Troponin Increased, Sputum Culture Positive, Multiple Drug Overdose, Tricuspid Valve Incompetence
Adverse event resulted in: hospitalization
Suspect drug(s):
Buspar
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Lorazepam
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Motrin
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Soma
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Ultram
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Other drugs received by patient: Claritin; Neurontin; Celexa; Phenazopyridine HCL TAB; Dalmane; Potassium Chloride
Adverse event in 55 year old female receiving Ultram (Tramadol)
Reported by a pharmacist from United States on 2007-06-18
Patient: 55 year old female, weighing 99.0 kg (217.8 pounds)
Adverse reactions / side effects: Confusional State, Muscle Rigidity
Adverse event resulted in: hospitalization
Suspect drug(s):
Ultram (Tramadol)
Other drugs received by patient: Indinavir; Nasonex; Advair Diskus 100 / 50; Neurontin; Zyprexa; Coreg; Megace; Clonidine; Hydralazine HCL; Zidovudine; Lamivudine; Coumadin; Doxepin HCL; Albuterol; Lortab; Lovenox; Avandia; Lotrel; Insulin; Altace
Adverse event in female receiving Ultram (Tramadol)
Reported by a physician from United States on 2007-05-29
Patient: female
Adverse reactions / side effects: Grand MAL Convulsion, Drug Interaction, Facial Bones Fracture, Fall
Adverse event resulted in: hospitalization
Suspect drug(s):
Rebif
Indication: Multiple Sclerosis
Ultram
Indication: Pain
Other drugs received by patient possibly interacting with the suspect drug:
Cymbalta
Indication: Drug USE FOR Unknown Indication
Adverse event in 57 year old female receiving Ultram (Tramadol)
Reported by a individual with unspecified qualification from United States on 2007-05-25
Patient: 57 year old female
Adverse reactions / side effects: Pneumonia Aspiration, Unresponsive TO Stimuli, Tricuspid Valve Incompetence, Somnolence, Foaming AT Mouth, Cyanosis, Sputum Culture Positive, Multiple Drug Overdose, Apnoea, Blood Glucose Increased, Blood Urea Increased, Blood Pressure Systolic Increased, Haemophilus Infection, Blood Chloride Increased, Troponin Increased, Streptococcal Infection, Aggression, Convulsion, Heart Rate Increased, Mitral Valve Incompetence
Adverse event resulted in: hospitalization
Suspect drug(s):
Buspar
Dosage: 33 tablets (5 mg tablets), oral
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Lorazepam
Dosage: 28 tablets (30mg tablets), oral
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Motrin
Dosage: 71 tablets (800 mg tablets), oral
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Soma (Carisoprodol, Usp) 350mg
Dosage: 87 tablets (350 mg tablets), oral
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Ultram
Dosage: 100 tablets, oral
Administration route: Oral
Start date: 2003-06-01
End date: 2003-06-01
Other drugs received by patient: Claritin; Neurontin; Celexa; Phenazopyridine HCL TAB; Dalmane; Potassium Chloride
Adverse event in female receiving Ultram (Tramadol)
Reported by a physician from United States on 2007-05-08
Patient: female
Adverse reactions / side effects: Grand MAL Convulsion, Facial Bones Fracture, Fall
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Cymbalta
Indication: Drug USE FOR Unknown Indication
Rebif
Indication: Multiple Sclerosis
Ultram
Indication: Pain
Adverse event in 32 year old female receiving Ultram (Tramadol)
Reported by a individual with unspecified qualification from United States on 2007-05-07
Patient: 32 year old female, weighing 59.9 kg (131.7 pounds)
Adverse reactions / side effects: Oedema Peripheral, Swelling, Hallucination, Tremor
Adverse event resulted in: hospitalization
Suspect drug(s):
Ultram (Tramadol)
Adverse event in 42 year old male receiving Ultram (Tramadol)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-02
Patient: 42 year old male, weighing 71.2 kg (156.6 pounds)
Adverse reactions / side effects: Angioedema, Wheezing
Adverse event resulted in: hospitalization
Suspect drug(s):
Flonase
Dosage: intranasal
Indication: Sinusitis
Start date: 2007-02-12
Loratadine
Dosage: 10 mg, qd, oral
Administration route: Oral
Indication: Hypersensitivity
Start date: 2007-02-12
Lotrel
Dosage: 5/20 mg, qd, oral
Administration route: Oral
Indication: Hypertension
Start date: 2007-02-12
End date: 2007-02-13
Ultram
Dosage: 50 mg
Indication: Pain
Start date: 2007-02-12
Adverse event in 39 year old male receiving Ultram (Tramadol)
Reported by a consumer/non-health professional from United States on 2007-04-26
Patient: 39 year old male
Adverse reactions / side effects: Drug Dependence
Adverse event resulted in: hospitalization
Suspect drug(s):
Ultram
Indication: Procedural Pain
Vicodin
Indication: Procedural Pain
Adverse event in 27 year old female receiving Ultram (Tramadol)
Reported by a physician from United States on 2007-04-23
Patient: 27 year old female
Adverse reactions / side effects: Pain, Coagulopathy, Injection Site Pain, Anticonvulsant Drug Level Decreased, Fall, Amnesia, Grand MAL Convulsion, Injection Site Erythema, Injection Site Induration, Injection Site Reaction, Facial Bones Fracture
Adverse event resulted in: hospitalization
Suspect drug(s):
Cymbalta
Start date: 2006-01-18
Rebif
Dosage: 44 mcg, 3 in 1 weeks, subcutaneous
Indication: Multiple Sclerosis
Start date: 2005-11-15
Ultram
Start date: 2006-01-18
End date: 2006-01-26
Adverse event in female receiving Ultram (Tramadol)
Reported by a physician from United States on 2007-04-20
Patient: female, weighing 69.8 kg (153.7 pounds)
Adverse reactions / side effects: Syncope, Affect Lability, Systemic Lupus Erythematosus, Headache, Feeling Drunk, Hallucination, Muscle Twitching, Tremor
Adverse event resulted in: hospitalization
Suspect drug(s):
Ultram (Tramadol)
Other drugs received by patient: Klonopin; Torodol
Adverse event in female receiving Ultram (Tramadol)
Reported by a physician from United States on 2007-04-06
Patient: female
Adverse reactions / side effects: Respiratory Failure, Multiple Drug Overdose
Adverse event resulted in: hospitalization
Suspect drug(s):
Buspar
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Lorazepam
Dosage: 30 mg, 28-30 total
Indication: Drug USE FOR Unknown Indication
Motrin
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Soma
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Ultram
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Flurazepam; Claritin; Neurontin; Celexa; Potassium Chloride; Acetaminophen and Hydrocodone Bitartrate
Adverse event in 41 year old female receiving Ultram (Tramadol)
Reported by a pharmacist from United States on 2007-03-02
Patient: 41 year old female, weighing 41.0 kg (90.2 pounds)
Adverse reactions / side effects: Pneumonia Aspiration, Incorrect Dose Administered, Atrial Fibrillation, Mental Status Changes, Convulsion
Adverse event resulted in: hospitalization
Suspect drug(s):
Ultram
Dosage: 1-2 -50mg- tablets q4-6 prn pain po (duration 1x; all at once)
Administration route: Oral
Indication: Pain
Wellbutrin
Dosage: po (duration: 1x; not patient's med)
Administration route: Oral
Indication: Self-Medication
Other drugs received by patient: Tramadol HCL; Fluoxetine
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