ALLI Side Effects

7022631-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Bilirubin Increased, Cholelithiasis, Hepatic Steatosis, Jaundice, Liver Injury, Scleral Discolouration, Serum Ferritin Increased
on Sep 28, 2010 Female patient from UNITED STATES , 52 years of age, was diagnosed with weight loss diet, multiple allergies and was treated with Alli (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, cholelithiasis, hepatic steatosis, jaundice (What is jaundice?), liver injury, scleral discolouration, serum ferritin increased. Alli dosage: . During the same period patient was treated with CLARITIN (View Claritin Review and Claritin Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ).

7020553-7 | Developmental Delay, Speech Disorder Developmental
Patient was taking Alli (View Usage). Patient had the following side effects: developmental delay, speech disorder developmental on Sep 24, 2010 from UNITED STATES Additional patient health information: Male patient , child 2 years of age, . Alli dosage: .

7019226-6 | Abdominal Pain Upper, Diverticulitis
Adverse event was reported on Sep 21, 2010 by a Female patient taking Alli (View Usage) (Dosage: ) . Location: FINLAND , 57 years of age, After Alli was administered, patient had the following side effects: abdominal pain upper, diverticulitis. Patient was hospitalized.

7019225-4 | Haematochezia
on Sep 17, 2010 Female patient from SPAIN , 55 years of age, was treated with Alli (View Usage). Patient experienced the following unwanted or unexpected effects: haematochezia. Alli dosage: .


7019224-2 | Abdominal Pain, Rectal Haemorrhage
on Sep 21, 2010 Female patient from SPAIN , 49 years of age, weighting 147.7 lb, was treated with Alli (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), rectal haemorrhage. Alli dosage: 120mg Per Day. During the same period patient was treated with IBUPROFEN TABLETS (View Ibuprofen Tablets Review and Ibuprofen Tablets Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).

7019223-0 | Blood Amylase Increased, Breast Pain, Defaecation Urgency, Fatigue, Frequent Bowel Movements, Lipase Increased, Pancreatitis Acute
Patient was taking Alli (View Usage). After Alli was administered, patient had the following side effects: blood amylase increased, breast pain, defaecation urgency, fatigue, frequent bowel movements, lipase increased, pancreatitis acute on Sep 23, 2010 from UNITED STATES Additional patient health information: Female patient , 65 years of age, weighting 154.3 lb, was diagnosed with weight loss diet and. Alli dosage: . Patient was hospitalized.

7016724-6 | Liver Disorder, Liver Injury
Adverse event was reported on Sep 21, 2010 by a Female patient taking Alli (View Usage) (Dosage: ) was diagnosed with constipation (What is constipation?) and. Location: UNITED STATES , 48 years of age, Patient experienced the following unwanted or unexpected effects: liver disorder, liver injury.

7016722-2 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Bilirubin Increased, Cholelithiasis, Hepatic Steatosis, Jaundice, Liver Injury, Scleral Discolouration, Serum Ferritin Increased
on Sep 21, 2010 Female patient from UNITED STATES , 52 years of age, was diagnosed with weight loss diet, multiple allergies and was treated with Alli (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, cholelithiasis, hepatic steatosis, jaundice (What is jaundice?), liver injury, scleral discolouration, serum ferritin increased. Alli dosage: . During the same period patient was treated with CLARITIN (View Claritin Review and Claritin Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ).

7016434-5 | Hyperamylasaemia
on Sep 16, 2010 Female patient from ITALY , 53 years of age, was treated with Alli (View Usage). After Alli was administered, patient had the following side effects: hyperamylasaemia. Alli dosage: 120mg Per Day. During the same period patient was treated with ALMARYTM (View Almarytm Review and Almarytm Label ).

7012667-2 | Metrorrhagia
Patient was taking Alli (View Usage). Patient experienced the following unwanted or unexpected effects: metrorrhagia on Sep 16, 2010 from FRANCE Additional patient health information: Female patient , weighting 235.9 lb, was diagnosed with contraception and. Alli dosage: 60mg Three Times Per Day. During the same period patient was treated with MICROVAL (View Microval Review and Microval Label ).

7010873-4 | Yellow Skin
Adverse event was reported on Sep 23, 2010 by a Female patient taking Alli (View Usage) (Dosage: See 8/31/2010 Report) . Location: UNITED STATES , 52 years of age, weighting 161.4 lb, Patient had the following side effects: yellow skin. Patient was hospitalized and became disabled.

6992679-5 | Flatulence, Gastrointestinal Hypermotility, Haemorrhoidal Haemorrhage, Haemorrhoids, Pain, Rectal Discharge
on Sep 09, 2010 Male patient from GREECE , 38 years of age, was diagnosed with obesity (What is obesity?) and was treated with Alli (View Usage). After Alli was administered, patient had the following side effects: flatulence, gastrointestinal hypermotility, haemorrhoidal haemorrhage, haemorrhoids, pain (What is pain?), rectal discharge. Alli dosage: 60mg Per Day.

6976746-8 | Gastric Disorder, Haematemesis, Nausea, Oropharyngeal Pain, Treatment Noncompliance
on Sep 09, 2010 Female patient from UNITED STATES , 46 years of age, was treated with Alli (View Usage). Patient experienced the following unwanted or unexpected effects: gastric disorder, haematemesis, nausea (What is nausea?), oropharyngeal pain, treatment noncompliance. Alli dosage: .

6976744-4 | Abdominal Pain Upper, Appendicectomy, Appendicitis
Patient was taking Alli (View Usage). Patient had the following side effects: abdominal pain upper, appendicectomy, appendicitis (What is appendicitis?) on Sep 08, 2010 from UNITED STATES Additional patient health information: Male patient , 42 years of age, was diagnosed with weight loss diet and. Alli dosage: . Patient was hospitalized.

6973554-9 | Hepatic Enzyme Increased, Oedema Peripheral
Adverse event was reported on Aug 20, 2010 by a Male patient taking Alli (View Usage) (Dosage: 60mg Twice Per Day) . Location: INDIA , 48 years of age, After Alli was administered, patient had the following side effects: hepatic enzyme increased, oedema peripheral. During the same period patient was treated with HYPERTENSION MED (View Hypertension Med Review and Hypertension Med Label ).

6973551-3 | Abdominal Discomfort, Abdominal Distension, Constipation, Flatulence, Obstruction Gastric, Product Quality Issue, Steatorrhoea
on Sep 07, 2010 Female patient from UNITED STATES , 53 years of age, was diagnosed with weight loss diet and was treated with Alli (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal discomfort, abdominal distension, constipation (What is constipation?), flatulence, obstruction gastric, product quality issue, steatorrhoea. Alli dosage: .

6970543-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Hepatic Enzyme Increased
on Aug 31, 2010 Female patient from UNITED STATES , 77 years of age, was treated with Alli (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, hepatic enzyme increased. Alli dosage: . During the same period patient was treated with TRACLEER (View Tracleer Review and Tracleer Label ), WARFARIN (View Warfarin Review and Warfarin Label ).

6962945-8 | Haematochezia
Patient was taking Alli (View Usage). After Alli was administered, patient had the following side effects: haematochezia on Aug 24, 2010 from GERMANY Additional patient health information: Female patient , 55 years of age, weighting 194.0 lb, . Alli dosage: 60mg See Dosage Text. During the same period patient was treated with LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ).

6962944-6 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Bilirubin Increased, Cholelithiasis, Hepatic Steatosis, Jaundice, Liver Injury, Scleral Discolouration, Serum Ferritin Increased
Adverse event was reported on Sep 01, 2010 by a Female patient taking Alli (View Usage) (Dosage: ) was diagnosed with weight loss diet, multiple allergies and. Location: UNITED STATES , 52 years of age, Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, cholelithiasis, hepatic steatosis, jaundice (What is jaundice?), liver injury, scleral discolouration, serum ferritin increased. During the same period patient was treated with CLARITIN (View Claritin Review and Claritin Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ).

6962136-0 | Arrhythmia, Cholelithiasis, Hepatic Steatosis, Hepatitis Acute
on Sep 01, 2010 Female patient from UNITED STATES , 52 years of age, weighting 161.0 lb, was diagnosed with weight control (What is weight control?) and was treated with Alli (View Usage). Patient had the following side effects: arrhythmia (What is arrhythmia?), cholelithiasis, hepatic steatosis, hepatitis acute. Alli dosage: . Patient was hospitalized.

6961217-5 | Haematochezia
on Aug 23, 2010 Female patient from AUSTRIA , 31 years of age, was treated with Alli (View Usage). After Alli was administered, patient had the following side effects: haematochezia. Alli dosage: .

6961215-1 | Breast Pain, Defaecation Urgency, Fatigue, Frequent Bowel Movements, Pancreatitis Acute
Patient was taking Alli (View Usage). Patient experienced the following unwanted or unexpected effects: breast pain, defaecation urgency, fatigue, frequent bowel movements, pancreatitis acute on Aug 31, 2010 from UNITED STATES Additional patient health information: Female patient , 65 years of age, weighting 154.3 lb, was diagnosed with weight loss diet and. Alli dosage: . Patient was hospitalized.

6958069-6 | Aphonia, Convulsion, Dysphagia
Adverse event was reported on Aug 30, 2010 by a Female patient taking Alli (View Usage) (Dosage: 60 Mg With Meal Po) was diagnosed with medical diet and. Location: UNITED STATES , 39 years of age, weighting 116.0 lb, Patient had the following side effects: aphonia, convulsion, dysphagia. Patient was hospitalized.

6956256-4 | Blood Urine Present, Haematochezia, Rectal Discharge
on Aug 27, 2010 Female patient from UNITED STATES , 38 years of age, was diagnosed with weight loss diet and was treated with Alli (View Usage). After Alli was administered, patient had the following side effects: blood urine present, haematochezia, rectal discharge. Alli dosage: .

6955926-1 | Abdominal Pain Lower, Irritable Bowel Syndrome
on Aug 26, 2010 Male patient from UNITED STATES , 50 years of age, weighting 270.0 lb, was diagnosed with weight control (What is weight control?) and was treated with Alli (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain lower, irritable bowel syndrome (What is irritable bowel syndrome?). Alli dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ).

6941454-6 | Thrombosis
Patient was taking Alli (View Usage). Patient had the following side effects: thrombosis on Aug 24, 2010 from UNITED STATES Additional patient health information: Female patient , 44 years of age, was diagnosed with weight loss diet and. Alli dosage: .

6941451-0 | Blood Magnesium Decreased, Blood Potassium Decreased, Blood Sodium Decreased, Electrolyte Imbalance, Heat Exhaustion, Vomiting
Adverse event was reported on Aug 23, 2010 by a Female patient taking Alli (View Usage) (Dosage: ) was diagnosed with weight loss diet and. Location: UNITED STATES , 56 years of age, weighting 232.6 lb, After Alli was administered, patient had the following side effects: blood magnesium decreased, blood potassium decreased, blood sodium decreased, electrolyte imbalance, heat exhaustion, vomiting. During the same period patient was treated with VITAMIN E (View Vitamin E Review and Vitamin E Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ). Patient was hospitalized.

6938849-3 | Rectal Haemorrhage
on Aug 13, 2010 Male patient from HUNGARY , 77 years of age, weighting 224.9 lb, was treated with Alli (View Usage). Patient experienced the following unwanted or unexpected effects: rectal haemorrhage. Alli dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), NITROMINT (View Nitromint Review and Nitromint Label ), DOXIUM (View Doxium Review and Doxium Label ), COVEREX (View Coverex Review and Coverex Label ), APO FAMOTIDINE (View Apo-famotidine Review and Apo-famotidine Label ), ACTRAPID (View Actrapid Review and Actrapid Label ).

6934209-X | Asthma, Bronchospasm, Dyspnoea
on Aug 12, 2010 Female patient from FRANCE , weighting 196.2 lb, was diagnosed with asthma (What is asthma?) and was treated with Alli (View Usage). Patient had the following side effects: asthma (What is asthma?), bronchospasm, dyspnoea. Alli dosage: . During the same period patient was treated with SINGULAIR (View Singulair Review and Singulair Label ). Patient was hospitalized.

6934208-8 | Haematochezia, Rectal Haemorrhage
Patient was taking Alli (View Usage). After Alli was administered, patient had the following side effects: haematochezia, rectal haemorrhage on Aug 12, 2010 from GREECE Additional patient health information: Female patient , 60 years of age, . Alli dosage: .

6930236-7 | Haematochezia
Adverse event was reported on Aug 10, 2010 by a Female patient taking Alli (View Usage) (Dosage: ) . Location: GERMANY , 55 years of age, Patient experienced the following unwanted or unexpected effects: haematochezia.

6930235-5 | Hepatic Enzyme Increased
on Aug 16, 2010 Female patient from UNITED STATES , 51 years of age, was diagnosed with weight loss diet and was treated with Alli (View Usage). Patient had the following side effects: hepatic enzyme increased. Alli dosage: .

6930234-3 | Blood Magnesium Decreased, Blood Potassium Decreased, Blood Sodium Decreased, Heat Exhaustion, Vomiting
on Aug 12, 2010 Female patient from UNITED STATES , 56 years of age, weighting 232.6 lb, was diagnosed with weight loss diet and was treated with Alli (View Usage). After Alli was administered, patient had the following side effects: blood magnesium decreased, blood potassium decreased, blood sodium decreased, heat exhaustion, vomiting. Alli dosage: . During the same period patient was treated with VITAMIN E (View Vitamin E Review and Vitamin E Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ). Patient was hospitalized.

6929311-2 | Contusion, Skin Atrophy, Skin Discolouration
Patient was taking Alli (View Usage). Patient experienced the following unwanted or unexpected effects: contusion, skin atrophy, skin discolouration on Aug 16, 2010 from UNITED STATES Additional patient health information: Female patient , 75 years of age, was diagnosed with weight loss diet and. Alli dosage: .

6929309-4 | Breast Pain, Defaecation Urgency, Fatigue, Frequent Bowel Movements, Pancreatitis Acute
Adverse event was reported on Aug 13, 2010 by a Female patient taking Alli (View Usage) (Dosage: ) was diagnosed with weight loss diet and. Location: UNITED STATES , 65 years of age, weighting 154.3 lb, Patient had the following side effects: breast pain, defaecation urgency, fatigue, frequent bowel movements, pancreatitis acute. Patient was hospitalized.

6919141-X | Haematochezia, Rectal Haemorrhage
on Aug 04, 2010 Female patient from GREECE , 60 years of age, was treated with Alli (View Usage). After Alli was administered, patient had the following side effects: haematochezia, rectal haemorrhage. Alli dosage: .

6919139-1 | Contusion, Skin Atrophy
on Aug 10, 2010 Female patient from UNITED STATES , 76 years of age, was diagnosed with weight loss diet and was treated with Alli (View Usage). Patient experienced the following unwanted or unexpected effects: contusion, skin atrophy. Alli dosage: .

6919138-X | Haematochezia
Patient was taking Alli (View Usage). Patient had the following side effects: haematochezia on Aug 10, 2010 from UNITED STATES Additional patient health information: Male patient , 48 years of age, was diagnosed with weight loss diet and. Alli dosage: .

6916902-8 | Eyelid Oedema, Product Quality Issue, Urinary Retention
Adverse event was reported on Jul 30, 2010 by a Male patient taking Alli (View Usage) (Dosage: 2cap Per Day) . Location: PORTUGAL , 46 years of age, weighting 231.5 lb, After Alli was administered, patient had the following side effects: eyelid oedema, product quality issue, urinary retention. During the same period patient was treated with LEXOTAN (48mg Per Day) (View Lexotan Review and Lexotan Label ), QUETIAPINE (450mg Per Day) (View Quetiapine Review and Quetiapine Label ).

6916899-0 | Asthma, Dyspnoea
on Jul 26, 2010 Female patient from UNITED STATES , 35 years of age, weighting 126.3 lb, was treated with Alli (View Usage). Patient experienced the following unwanted or unexpected effects: asthma (What is asthma?), dyspnoea. Alli dosage: . During the same period patient was treated with CYCLOBENZAPRINE HCL (View Cyclobenzaprine Hcl Review and Cyclobenzaprine Hcl Label ), OMEPRAZOLE (20mg Per Day) (View Omeprazole Review and Omeprazole Label ), BUPROPION HCL (View Bupropion Hcl Review and Bupropion Hcl Label ), XANAX (View Xanax Review and Xanax Label ), CITALOPRAM HYDROBROMIDE (View Citalopram Hydrobromide Review and Citalopram Hydrobromide Label ), METFORMIN HCL (500mg Twice Per Day) (View Metformin Hcl Review and Metformin Hcl Label ), DICYCLOMINE (View Dicyclomine Review and Dicyclomine Label ), HYDROCORTISONE + LIDOCAINE (View Hydrocortisone + Lidocaine Review and Hydrocortisone + Lidocaine Label ).

6914093-0 | Haematochezia
on Aug 06, 2010 Female patient from UNITED STATES , 32 years of age, was diagnosed with weight loss diet and was treated with Alli (View Usage). Patient had the following side effects: haematochezia. Alli dosage: .

6913443-9 | Diverticulitis
Patient was taking Alli (View Usage). After Alli was administered, patient had the following side effects: diverticulitis on Aug 05, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 175.0 lb, was diagnosed with weight control (What is weight control?) and. Alli dosage: 60 Mg 3 X Daily. Patient was hospitalized.

6908865-6 | Rectal Haemorrhage
Adverse event was reported on Jul 29, 2010 by a Male patient taking Alli (View Usage) (Dosage: ) . Location: HUNGARY , 77 years of age, weighting 224.9 lb, Patient experienced the following unwanted or unexpected effects: rectal haemorrhage. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), NITROMINT (View Nitromint Review and Nitromint Label ), DOXIUM (View Doxium Review and Doxium Label ), COVEREX (View Coverex Review and Coverex Label ), APO FAMOTIDINE (View Apo-famotidine Review and Apo-famotidine Label ), ACTRAPID (View Actrapid Review and Actrapid Label ).

6908863-2 | Chest Pain, Cholecystectomy, Dyspepsia, Gallbladder Disorder, Hepatic Infection, Malaise
on Aug 04, 2010 Female patient from UNITED STATES , 43 years of age, was diagnosed with weight loss diet and was treated with Alli (View Usage). Patient had the following side effects: chest pain (What is chest pain?), cholecystectomy, dyspepsia, gallbladder disorder, hepatic infection, malaise. Alli dosage: . During the same period patient was treated with MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ). Patient was hospitalized.

6906301-7 | Headache, Rectal Haemorrhage, Vaginal Haemorrhage
on Aug 03, 2010 Female patient from UNITED STATES , 35 years of age, was diagnosed with weight loss diet and was treated with Alli (View Usage). After Alli was administered, patient had the following side effects: headache (What is headache?), rectal haemorrhage, vaginal haemorrhage. Alli dosage: .

6902492-2 | Colon Cancer
Patient was taking Alli (View Usage). Patient experienced the following unwanted or unexpected effects: colon cancer on Aug 02, 2010 from UNITED STATES Additional patient health information: Male patient , 57 years of age, weighting 170.0 lb, was diagnosed with weight control (What is weight control?) and. Alli dosage: .

6901016-3 | Chest Pain, Hepatic Enzyme Increased, Hepatomegaly, Liver Disorder
Adverse event was reported on Aug 02, 2010 by a Female patient taking Alli (View Usage) (Dosage: ) was diagnosed with weight loss diet, blood cholesterol increased and. Location: UNITED STATES , 45 years of age, Patient had the following side effects: chest pain (What is chest pain?), hepatic enzyme increased, hepatomegaly, liver disorder. During the same period patient was treated with XENICAL (2cap Cumulative Dose) (View Xenical Review and Xenical Label ), PRAVASTATIN (25mg Per Day) (View Pravastatin Review and Pravastatin Label ). Patient was hospitalized.

6895878-6 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Diarrhoea, Gamma-glutamyltransferase Increased
on Jul 26, 2010 Female patient from BELGIUM , 38 years of age, was diagnosed with weight decreased, type 1 diabetes mellitus and was treated with Alli (View Usage). After Alli was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, diarrhoea, gamma-glutamyltransferase increased. Alli dosage: 1tab Per Day. During the same period patient was treated with INSULINE (4inj Per Day) (View Insuline Review and Insuline Label ), CONTRACEPTIVE IMPLANT (View Contraceptive Implant Review and Contraceptive Implant Label ).

6895877-4 | Chest Pain, Hepatic Enzyme Increased, Hepatomegaly, Liver Disorder
on Jul 30, 2010 Female patient from UNITED STATES , 45 years of age, was diagnosed with weight loss diet, blood cholesterol increased and was treated with Alli (View Usage). Patient experienced the following unwanted or unexpected effects: chest pain (What is chest pain?), hepatic enzyme increased, hepatomegaly, liver disorder. Alli dosage: . During the same period patient was treated with XENICAL (2cap Cumulative Dose) (View Xenical Review and Xenical Label ), PRAVASTATIN (25mg Per Day) (View Pravastatin Review and Pravastatin Label ). Patient was hospitalized.

6895418-1 | Blood Bilirubin Increased, Diarrhoea, Effusion, Faeces Pale, Gallbladder Disorder, Hepatic Enzyme Increased, Jaundice, Pruritus, Scab
Patient was taking Alli (View Usage). Patient had the following side effects: blood bilirubin increased, diarrhoea, effusion, faeces pale, gallbladder disorder, hepatic enzyme increased, jaundice (What is jaundice?), pruritus, scab (What is scab?) on Jul 30, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 253.0 lb, was diagnosed with weight increased and. Alli dosage: One Pill After Each Meal Po. During the same period patient was treated with FOSRENOL (View Fosrenol Review and Fosrenol Label ), ELIPHOS (View Eliphos Review and Eliphos Label ), CARVEDILOL (View Carvedilol Review and Carvedilol Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), DIOVAN (View Diovan Review and Diovan Label ), GEODON (View Geodon Review and Geodon Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), TOPRIAMATE (View Topriamate Review and Topriamate Label ).