Fibromyalgia, Jaw Disorder, Temporomandibular Joint Syndrome, Arthritis, Arthralgia (8506567-6)
on Feb 20, 2009 Female patient from UNITED STATES , 76 years of age, was treated with Ultram(View Usage). Patient experienced the following unwanted or unexpected effects: fibromyalgia, jaw disorder, temporomandibular joint syndrome, arthritis (arthritis Questions), arthralgia. Ultram dosage: N/A.
Patient was taking other medications:

• RECLAST (Infusion) (View Reclast Review and Reclast Label )

Pain In Extremity, Arthralgia, Bone Pain, Eye Pain, Gait Disturbance (8501839-3)
Patient was taking Ultram (View Usage). Patient had the following side effects: pain in extremity, arthralgia, bone pain, eye pain, gait disturbance on Aug 23, 2010 from UNITED STATES Additional patient health information: Female patient , 68 years of age, weighting 162.0 lb, . Ultram dosage: N/A.
Patient was taking other medications:

• RECLAST (5 Mg, Iv Infusion) (View Reclast Review and Reclast Label )

Intervertebral Disc Protrusion, Maternal Exposure During Pregnancy, Neck Pain (8475943-2)
Adverse event was reported on Jun 15, 2012 by a Female patient taking Ultram Er (View Usage) (Dosage: Once Daily (200 Mg Out Of 300 Mg)) . Location: UNITED STATES , weighting 125.0 lb, After Ultram was administered, patient had the following side effects: intervertebral disc protrusion, maternal exposure during pregnancy, neck pain.
Patient was taking other medications:

• NORCO (View Norco Review and Norco Label )

Patient was hospitalized.

Gastroenteritis Norovirus, Renal Failure, Dehydration (8464270-5)
on Jun 18, 2012 Female patient from UNITED STATES , weighting 175.0 lb, was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: gastroenteritis norovirus, renal failure, dehydration. Ultram dosage: 50 Mg, 2x/day.
Patient was taking other medications:

• ALBUTEROL (2 Puffs Ever 6 Hours As Needed) (View Albuterol Review and Albuterol Label )
• AMITRIPTYLINE (1 Tablet (50 Mg) Every Day At Bedtime) (View Amitriptyline Review and Amitriptyline Label )
• XANAX (0.25 Mg, 3x/day) (View Xanax Review and Xanax Label )
• PRISTIQ (50 Mg, 1x/day) (View Pristiq Review and Pristiq Label )
• SYNTHROID (125 Ug, 1x/day) (View Synthroid Review and Synthroid Label )
• SYMBICORT (2 Puffs Two Times Every Day In The Morning And Evening) (View Symbicort Review and Symbicort Label )
• ZYRTEC (10 Mg, 1x/day) (View Zyrtec Review and Zyrtec Label )

Patient was hospitalized.


Rash, Diarrhoea, Dermatitis, Hypocalcaemia (8437163-7)
on Mar 01, 2012 Male patient from UNITED STATES , 89 years of age, weighting 127.0 lb, was treated with Ultram(View Usage). Patient had the following side effects: rash (rash Questions), diarrhoea, dermatitis, hypocalcaemia. Ultram dosage: N/A.
Patient was taking other medications:

• CALCIUM (800 Mg, Qd) (View Calcium Review and Calcium Label )
• LEUCOVORIN CALCIUM (View Leucovorin Calcium Review and Leucovorin Calcium Label )
• REMERON (15 Mg, Qhs) (View Remeron Review and Remeron Label )
• ASPIRIN (81 Mg, Qd) (View Aspirin Review and Aspirin Label )
• VITAMIN D (600 Iu, Qd) (View Vitamin D Review and Vitamin D Label )
• FINASTERIDE (View Finasteride Review and Finasteride Label )
• NEXIUM (View Nexium Review and Nexium Label )
• COLCHICINE (View Colchicine Review and Colchicine Label )

Myocardial Infarction, Withdrawal Syndrome (8435688-1)
Patient was taking Ultram Er (View Usage). After Ultram was administered, patient had the following side effects: myocardial infarction, withdrawal syndrome on Jun 08, 2012 from UNITED STATES Additional patient health information: Female patient , weighting 120.0 lb, was diagnosed with

• arthralgia

and. Ultram Er dosage: Once A Day.
Patient was taking other medications:

• HUMALOG (View Humalog Review and Humalog Label )

Patient was hospitalized.

Oedema Peripheral, Nausea, Hypersensitivity (8431690-4)
Adverse event was reported on Jun 05, 2012 by a Female patient taking Ultram (View Usage) (Dosage: N/A) . Location: UNITED STATES , weighting 145.0 lb, Patient experienced the following unwanted or unexpected effects: oedema peripheral, nausea (nausea Questions), hypersensitivity.
Patient was taking other medications:

• NAPROXEN (View Naproxen Review and Naproxen Label )
• BACLOFEN (View Baclofen Review and Baclofen Label )
• CHANTIX (View Chantix Review and Chantix Label )

Joint Range Of Motion Decreased (8418818-7)
on Jun 04, 2012 Female patient from UNITED STATES , weighting 196.2 lb, was diagnosed with

• pain (pain Questions)
• neuropathy peripheral
• pain in extremity

and was treated with Ultram (View Usage). Patient had the following side effects: joint range of motion decreased. Ultram dosage: 100 Mg, As Needed.
Patient was taking other medications:

• LYRICA (100 Mg, 4x/day) (View Lyrica Review and Lyrica Label )

Burning Sensation, Urticaria, Pruritus, Blister (8417934-3)
on Jun 01, 2012 Female patient from UNITED STATES , weighting 130.0 lb, was diagnosed with

• pain (pain Questions)

and was treated with Ultram(View Usage). After Ultram was administered, patient had the following side effects: burning sensation, urticaria, pruritus, blister. Ultram dosage: One Every 6 Hrs On Demand.

Joint Injury, Fall, Osteoporosis, Wrist Fracture (8417692-2)
Patient was taking Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: joint injury, fall (fall Questions), osteoporosis (osteoporosis Questions), wrist fracture on May 29, 2012 from UNITED STATES Additional patient health information: Female patient , 31 years of age, weighting 136.0 lb, . Ultram dosage: N/A.
Patient was taking other medications:

• NEXIUM (View Nexium Review and Nexium Label )

Patient was hospitalized.

Chest Pain, Dyspnoea, Heart Rate Decreased (8387070-3)
Adverse event was reported on May 23, 2012 by a Male patient taking Ultram (View Usage) (Dosage: 50 Mg Bid) was diagnosed with

• arthralgia

and. Location: UNITED STATES , 61 years of age, weighting 182.0 lb, Patient had the following side effects: chest pain (chest pain Questions), dyspnoea, heart rate decreased.

Swelling, Pruritus, Pyrexia, Hypersensitivity, Rash (8367095-4)
on Sep 09, 2011 Female patient from UNITED STATES , 50 years of age, was treated with Ultram (tramdol Hydrochloride) (View Usage). After Ultram was administered, patient had the following side effects: swelling, pruritus, pyrexia, hypersensitivity, rash (rash Questions). Ultram (tramdol Hydrochloride) dosage: N/A.
Patient was taking other medications:

• ACYCLOVIR (View Acyclovir Review and Acyclovir Label )
• PREDNISONE (PREDISONE) (View Prednisone (predisone) Review and Prednisone (predisone) Label )
• ALOXI (PALODOSETRON HYDROCHLORIDE) (View Aloxi (palodosetron Hydrochloride) Review and Aloxi (palodosetron Hydrochloride) Label )
• VELCADE (View Velcade Review and Velcade Label )
• REVLIMID (See Image) (View Revlimid Review and Revlimid Label )

Lymphadenopathy, Gastritis, Hepatic Steatosis, Gastric Mucosal Hypertrophy, Gastric Antral Vascular Ectasia (8360579-4)
on May 11, 2012 Female patient from UNITED STATES , weighting 181.9 lb, was diagnosed with

• headache (headache Questions)
• pain (pain Questions)
• gastrooesophageal reflux disease

and was treated with Ultram(View Usage). Patient experienced the following unwanted or unexpected effects: lymphadenopathy, gastritis, hepatic steatosis, gastric mucosal hypertrophy, gastric antral vascular ectasia. Ultram dosage: 50-100 Mg Prn.
Patient was taking other medications:

• TRAMADOL HYDROCHLORIDE (Unk Ukn, Unk) (View Tramadol Hydrochloride Review and Tramadol Hydrochloride Label )
• ESOMEPRAZOLE MAGNESIUM (40 Mg, Bid) (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label )
• IBUPROFEN (200 Mg, Prn) (View Ibuprofen Review and Ibuprofen Label )
• GILENYA (0.5 Mg, Qd) (View Gilenya Review and Gilenya Label )
• GABAPENTIN (400 Mg, Bid) (View Gabapentin Review and Gabapentin Label )
• SERTRALINE HYDROCHLORIDE (100 Mg, Qd) (View Sertraline Hydrochloride Review and Sertraline Hydrochloride Label )
• PREGABALIN (75 Mg, Bid) (View Pregabalin Review and Pregabalin Label )

Thrombocytopenia, Oesophageal Ulcer, Oesophageal Ulcer Haemorrhage (8350770-5)
Patient was taking Ultram (View Usage). Patient had the following side effects: thrombocytopenia, oesophageal ulcer, oesophageal ulcer haemorrhage on May 08, 2012 from UNITED STATES Additional patient health information: Female patient , 76 years of age, weighting 147.7 lb, . Ultram dosage: N/A. Patient was hospitalized.

Cardiac Failure Congestive, Atrial Fibrillation (8338615-0)
Adverse event was reported on Apr 23, 2012 by a Female patient taking Ultram (View Usage) (Dosage: N/A) . Location: UNITED STATES , weighting 159.4 lb, After Ultram was administered, patient had the following side effects: cardiac failure congestive, atrial fibrillation (atrial fibrillation Questions).
Patient was taking other medications:

• EFFEXOR XR (View Effexor Xr Review and Effexor Xr Label )
• GAMMAGARD LIQUID (View Gammagard Liquid Review and Gammagard Liquid Label )
• EXELON (View Exelon Review and Exelon Label )
• GLUCERNA ^ABBOTT^ (View Glucerna ^abbott^ Review and Glucerna ^abbott^ Label )

Patient was hospitalized.

Lung Neoplasm, Cough, Chest Pain, Adverse Event, Osteoarthritis (8334160-7)
on Apr 24, 2012 Female patient from UNITED STATES , 60 years of age, was diagnosed with

• pain (pain Questions)

and was treated with Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: lung neoplasm, cough, chest pain (chest pain Questions), adverse event, osteoarthritis (osteoarthritis Questions). Ultram dosage: 50-100 Mg Every For Hours As Needed.
Patient was taking other medications:

• ATACAND (View Atacand Review and Atacand Label )
• TENORMIN (View Tenormin Review and Tenormin Label )
• ASPIRIN (View Aspirin Review and Aspirin Label )
• ZESTRIL (View Zestril Review and Zestril Label )
• NORVASC (View Norvasc Review and Norvasc Label )

Patient was hospitalized.

Speech Disorder, Abnormal Behaviour (8320286-0)
on Apr 26, 2012 Female patient from UNITED STATES , 70 years of age, weighting 170.0 lb, was diagnosed with

• pain (pain Questions)

and was treated with Ultram(View Usage). Patient had the following side effects: speech disorder, abnormal behaviour. Ultram dosage: 50mg 2x Day.

Condition Aggravated, Oedema Peripheral, Laceration, Cervical Spinal Stenosis, Medical Device Complication, Tenderness, Contusion, Arthralgia, Device Dislocation (8293806-2)
Patient was taking Ultram (tamadol Hydrochloride) (View Usage). After Ultram was administered, patient had the following side effects: condition aggravated, oedema peripheral, laceration, cervical spinal stenosis, medical device complication, tenderness, contusion, arthralgia, device dislocation on Mar 29, 2012 from UNITED STATES Additional patient health information: Female patient , 70 years of age, weighting 120.0 lb, . Ultram (tamadol Hydrochloride) dosage: N/A.
Patient was taking other medications:

• ASPIRIN (View Aspirin Review and Aspirin Label )
• GLUCOSAMINE (GLUCOSAMINE) (View Glucosamine (glucosamine) Review and Glucosamine (glucosamine) Label )
• CALCIUM CARBONATE (View Calcium Carbonate Review and Calcium Carbonate Label )
• PREMARIN (ESTOGRENS CONJUGATED) (View Premarin (estogrens Conjugated) Review and Premarin (estogrens Conjugated) Label )
• EXTRA STRENGTH TYLENOL (View Extra Strength Tylenol Review and Extra Strength Tylenol Label )
• ANESTHETICS, LOCAL (ANESTHETICS, LOCAL) (View Anesthetics, Local (anesthetics, Local) Review and Anesthetics, Local (anesthetics, Local) Label )
• XIAFLEX (Intralesional) (View Xiaflex Review and Xiaflex Label )
• SIMVASTATIN (View Simvastatin Review and Simvastatin Label )

Patient was hospitalized.

Condition Aggravated (8292764-4)
Adverse event was reported on Apr 04, 2011 by a Female patient taking Ultram (View Usage) (Dosage: N/A) was diagnosed with

• back pain (back pain Questions)
• anxiety (anxiety Questions)

and. Location: UNITED STATES , 59 years of age, weighting 140.0 lb, Patient experienced the following unwanted or unexpected effects: condition aggravated.
Patient was taking other medications:

• LORAZEPAM (View Lorazepam Review and Lorazepam Label )
• PREMPRO (View Prempro Review and Prempro Label )
• TRIAMETERENE HCTZ (View Triameterene Hctz Review and Triameterene Hctz Label )
• NEXIUM (View Nexium Review and Nexium Label )

Spinal Compression Fracture, Fall (8276034-6)
on Mar 28, 2012 Female patient from UNITED STATES , weighting 135.0 lb, was diagnosed with

• pain (pain Questions)

and was treated with Ultram (View Usage). Patient had the following side effects: spinal compression fracture, fall (fall Questions). Ultram dosage: N/A.

Nausea, Malaise (8257912-0)
on Mar 30, 2012 Female patient from UNITED STATES , weighting 200.0 lb, was treated with Ultram(View Usage). After Ultram was administered, patient had the following side effects: nausea (nausea Questions), malaise. Ultram dosage: Unk.
Patient was taking other medications:

• LEVOTHYROXINE (Unk) (View Levothyroxine Review and Levothyroxine Label )
• HYDROCODONE (Unk) (View Hydrocodone Review and Hydrocodone Label )
• LYRICA (100 Mg, 3x/day) (View Lyrica Review and Lyrica Label )

Blood Bilirubin Increased, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased (8251774-3)
Patient was taking Ultram (View Usage). Patient experienced the following unwanted or unexpected effects: blood bilirubin increased, alanine aminotransferase increased, aspartate aminotransferase increased on Mar 27, 2012 from UNITED STATES Additional patient health information: Male patient , weighting 155.0 lb, . Ultram dosage: Unk.
Patient was taking other medications:

• LORTAB (Unk) (View Lortab Review and Lortab Label )
• ALBUTEROL (Unk) (View Albuterol Review and Albuterol Label )
• HALDOL (Unk) (View Haldol Review and Haldol Label )
• FOLIC ACID (Unk) (View Folic Acid Review and Folic Acid Label )
• CATAPRES (Unk) (View Catapres Review and Catapres Label )
• DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER (5 %, Unk) (View Dextrose 5% And Sodium Chloride 0.45% In Plastic Container Review and Dextrose 5% And Sodium Chloride 0.45% In Plastic Container Label )
• VISTARIL (Unk) (View Vistaril Review and Vistaril Label )
• ZOFRAN (Unk) (View Zofran Review and Zofran Label )

Nausea, Mallory-weiss Syndrome, Oesophageal Haemorrhage (8249985-6)
Adverse event was reported on Mar 28, 2012 by a Male patient taking Ultram (View Usage) (Dosage: N/A) was diagnosed with

• pain (pain Questions)
• knee arthroplasty

and. Location: UNITED STATES , weighting 185.0 lb, Patient had the following side effects: nausea (nausea Questions), mallory-weiss syndrome, oesophageal haemorrhage. Patient was hospitalized.

Tinnitus (8234282-5)
on Mar 19, 2012 Female patient from CANADA , 54 years of age, was treated with Ultram (View Usage). After Ultram was administered, patient had the following side effects: tinnitus (tinnitus Questions). Ultram dosage: 3-4 Times Per Day As Needed..

Pruritus, Hypersensitivity (8233182-4)
on Mar 22, 2012 Female patient from UNITED STATES , weighting 251.0 lb, was treated with Ultram(View Usage). Patient experienced the following unwanted or unexpected effects: pruritus, hypersensitivity. Ultram dosage: Unk.
Patient was taking other medications:

• AMITRIPTYLINE (Unk) (View Amitriptyline Review and Amitriptyline Label )
• SPIRIVA (Unk) (View Spiriva Review and Spiriva Label )
• CHANTIX (0.5 Mg, 2x/day) (View Chantix Review and Chantix Label )