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Ultram (Tramadol) - Adverse Event Reports - All Cases

 



Index of reports > All cases (50)

     Convulsion (6)Drug Ineffective (5)Unresponsive TO Stimuli (3)Headache (3)Grand MAL Convulsion (3)Overdose (3)Respiratory Failure (3)Completed Suicide (3)Facial Bones Fracture (3)Pharmaceutical Product Complaint (3)

Below is the selection of adverse event reports related to Ultram (Tramadol) that includes all cases.

 Reports 1 - 25 of 50   Next >>

Adverse event in 65 year old female receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-10-25

Patient: 65 year old female

Adverse reactions / side effects: Drug Ineffective, Underdose, Blindness Unilateral

Suspect drug(s):
Ultram (Tramadol)



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 64 year old female receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-10-23

Patient: 64 year old female, weighing 61.2 kg (134.7 pounds)

Adverse reactions / side effects: Acne

Suspect drug(s):
Ultram (Tramadol)



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 female receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-10-19

Patient: female, weighing 62.6 kg (137.7 pounds)

Adverse reactions / side effects: Daydreaming, Flight of Ideas, Amnesia

Suspect drug(s):
Chantix
    Administration route: Oral
    Indication: Smoking Cessation Therapy
    Start date: 2007-09-27
    End date: 2007-10-05

Amoxicillin
    Indication: Pneumonia
    Start date: 2007-01-01
    End date: 2007-10-05

Ultram
    Indication: Pneumonia
    Start date: 2007-01-01
    End date: 2007-10-05



Adverse event in female receiving Ultram (Tramadol)

Reported by a individual with unspecified qualification from United States on 2007-10-12

Patient: female, weighing 82.1 kg (180.6 pounds)

Adverse reactions / side effects: Drug Effect Decreased, Therapeutic Response Unexpected With Drug Substitution, Inadequate Analgesia

Suspect drug(s):
Ultram (Tramadol)



Adverse event in female receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-10-09

Patient: female

Adverse reactions / side effects: Convulsion

Suspect drug(s):
Ultram ER
    Dosage: 1 in 1 day, oral
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Ultram
    Dosage: 1 in 1 d, oral
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in female receiving Ultram (Tramadol)

Reported by a physician from United States on 2007-10-09

Patient: female

Adverse reactions / side effects: Drug Ineffective, Pharmaceutical Product Complaint

Suspect drug(s):
Ultram (Tramadol)



Adverse event in female receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-10-03

Patient: female, weighing 57.7 kg (127.0 pounds)

Adverse reactions / side effects: Impaired Driving Ability, Sleep Disorder, DRY Mouth, Dizziness, Rash, Tooth Disorder

Suspect drug(s):
Lyrica
    Indication: Fibromyalgia

Lyrica
    Indication: Neuropathy

Neurontin

Clonazepam
    Indication: Sleep Disorder

Methadone HCL
    Indication: Pain

Ultram

Other drugs received by patient: Fosamax; Soma



Adverse event in 52 year old male receiving Ultram (Tramadol)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-20

Patient: 52 year old male, weighing 72.6 kg (159.7 pounds)

Adverse reactions / side effects: Pruritus, Urticaria, Gastric Disorder

Adverse event resulted in: disablity

Suspect drug(s):
Ultram (Tramadol)



Adverse event in 28 year old male receiving Ultram (Tramadol)

Reported by a physician from United States on 2007-07-18

Patient: 28 year old male

Adverse reactions / side effects: Death, Opiates Positive

Adverse event resulted in: death

Suspect drug(s):
Ultram ER
    Administration route: Oral

Ultram ER
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Ultram
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in male receiving Ultram (Tramadol)

Reported by a physician from United States on 2007-07-16

Patient: male, weighing 134.3 kg (295.4 pounds)

Adverse reactions / side effects: Drug Toxicity, Analgesic Drug Level Above Therapeutic, Overdose, Completed Suicide

Adverse event resulted in: death

Suspect drug(s):
Ultram
    Administration route: Oral
    Indication: Arthralgia

Ultram
    Administration route: Oral

Other drugs received by patient: Benicar HCT; Keppra; VIT BIZ; Carafate; Zocor; Claritin; Protonix



Adverse event in male receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-07-13

Patient: male, weighing 72.6 kg (159.7 pounds)

Adverse reactions / side effects: Pruritus, Urticaria

Adverse event resulted in: disablity

Suspect drug(s):
Ultram (Tramadol)



Adverse event in 89 year old female receiving Ultram (Tramadol)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-13

Patient: 89 year old female, weighing 68.2 kg (150.0 pounds)

Adverse reactions / side effects: HIP Fracture, Hyponatraemia, Post Procedural Infection

Suspect drug(s):
Norvasc
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Deltasone
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Aldactone
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Bextra
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Remeron
    Administration route: Oral
    Indication: Depression

Effexor XR
    Dosage: daily dose:225mg-freq:unknown
    Administration route: Oral
    Indication: Depression

Advair Diskus 100 / 50
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Ultram
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Tylenol
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Docusate Sodium
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Aspirin
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Pepcid
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Lovenox
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Ancef
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Trazodone HCL
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Lasix
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Keflex
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

SLO-MAG
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

PRO-Banthine
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Coreg
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Cozaar
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Darvocet
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Duoneb
    Dosage: text:unknown-freq:unknown
    Indication: Drug USE FOR Unknown Indication

Bucindolol Hydrochloride
    Dosage: text:unknown
    Indication: Drug USE FOR Unknown Indication



Adverse event in female receiving Ultram (Tramadol)

Reported by a pharmacist from United States on 2007-07-09

Patient: female

Adverse reactions / side effects: Trismus, Nightmare

Suspect drug(s):
Ultram (Tramadol)

Other drugs received by patient: Metoprolol Succinate; Maxzide; Vigamox



Adverse event in female receiving Ultram (Tramadol)

Reported by a pharmacist from United States on 2007-07-09

Patient: female

Adverse reactions / side effects: Trismus, Nightmare

Suspect drug(s):
Ultram (Tramadol)



Adverse event in male receiving Ultram (Tramadol)

Reported by a pharmacist from United States on 2007-06-27

Patient: male, weighing 13.0 kg (28.6 pounds)

Adverse reactions / side effects: Unresponsive TO Stimuli, Respiratory Depression

Suspect drug(s):
Ultram (Tramadol)

Other drugs received by patient: Chloral Hydrate; Amitriptyline HCL; Tylenol; Zyrtec; Clonidine; Cyproheptadine HCL; Diazepam; Diazepam; Gabapentin; Ibuprofen; Zantac; Zonegran; Prevacid



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

Motrin
    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

Soma
    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

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 2007-06-19

Patient: female, weighing 64.9 kg (142.7 pounds)

Adverse reactions / side effects: Accident, Hypoglycaemia, Analgesic Drug Level, Convulsion

Suspect drug(s):
Ultram
    Administration route: Oral

Ultram
    Dosage: 50mg every 4 hours as needed, up to 8 tablets per day
    Administration route: Oral
    Indication: Fibromyalgia

Other drugs received by patient: Suboxone; Ativan



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 47 year old female receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-06-08

Patient: 47 year old female

Adverse reactions / side effects: Visual Acuity Reduced, Optic Nerve Injury, Eye Pain

Suspect drug(s):
Ultram (Tramadol)



Adverse event in male receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-06-07

Patient: male, weighing 68.0 kg (149.7 pounds)

Adverse reactions / side effects: Overdose, Drug Withdrawal Syndrome, Self-Medication, Convulsion

Suspect drug(s):
Ultram (Tramadol)

Other drugs received by patient: Effexor; Effexor; Neurontin



Adverse event in female receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-06-07

Patient: female, weighing 104.3 kg (229.5 pounds)

Adverse reactions / side effects: Headache, Intracranial Pressure Increased

Suspect drug(s):
Ultram
    Administration route: Oral
    Indication: Fibromyalgia

Ultram
    Administration route: Oral
    Indication: Pain

Other drugs received by patient: Metaformin; Singulair; Lyrica; Synthroid; Invega; Topamax; Cymbalta; Aciphex; Zyrtec; Zanaflex



Adverse event in 37 year old female receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-06-07

Patient: 37 year old female

Adverse reactions / side effects: Road Traffic Accident, Altered Visual Depth Perception

Suspect drug(s):
Ultram (Tramadol)



Adverse event in female receiving Ultram (Tramadol)

Reported by a consumer/non-health professional from United States on 2007-06-07

Patient: female

Adverse reactions / side effects: Drug Ineffective, Alopecia

Suspect drug(s):
Ultram
    Indication: Drug USE FOR Unknown Indication

Plavix
    Indication: Drug USE FOR Unknown Indication



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