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FDA Adverse Reports: 70. View All

Lopid FDA safety alerts: 2009

Reported hospitalizations: 13

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Often additional risks of using a medication, such as Lopid, 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 Lopid users, Learn more about unwanted side effects & find ways to reduce them. Browse Lopid Adverse Reports reported to FDA and participate in Lopid discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Lopid. 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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Lopid Adverse Effect Reports (FDA)

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7010081-7 | Rhabdomyolysis
on Jul 28, 2009 Male patient from UNITED STATES , 50 years of age, was treated with Lopid (View Usage). Patient experienced the following unwanted or unexpected effects: rhabdomyolysis. Lopid dosage: 600 Mg, 2x/day. During the same period patient was treated with FENOFIBRIC ACID (135 Mg) (View Fenofibric Acid Review and Fenofibric Acid Label ), DILANTIN (View Dilantin Review and Dilantin Label ), PHENOBARBITAL TAB (View Phenobarbital Tab Review and Phenobarbital Tab Label ). Patient was hospitalized.

7003373-9 | Diarrhoea
Patient was taking Lopid (View Usage). Patient had the following side effects: diarrhoea on Sep 08, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 216.1 lb, was diagnosed with blood triglycerides increased and. Lopid dosage: 600 Mg, 2x/day. During the same period patient was treated with ACETYLSALICYLIC ACID (Unk) (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), BISOPROLOL (Unk) (View Bisoprolol Review and Bisoprolol Label ), COENZYME Q10 (Unk) (View Coenzyme Q10 Review and Coenzyme Q10 Label ), CRESTOR (Unk) (View Crestor Review and Crestor Label ), FISH OIL (Unk) (View Fish Oil Review and Fish Oil Label ), FLONASE (Unk) (View Flonase Review and Flonase Label ), LISINOPRIL AND HYDROCHLOROTHIAZIDE (Unk) (View Lisinopril And Hydrochlorothiazide Review and Lisinopril And Hydrochlorothiazide Label ), LORATADINE (Unk) (View Loratadine Review and Loratadine Label ).

6970916-0 | Osteoarthritis, Renal Failure
Adverse event was reported on Aug 24, 2010 by a Female patient taking Lopid (View Usage) (Dosage: Unk) was diagnosed with blood triglycerides increased, hypertension, arthralgia and. Location: COLOMBIA , 80 years of age, After Lopid was administered, patient had the following side effects: osteoarthritis (What is osteoarthritis?), renal failure. During the same period patient was treated with OLMETEC (1 Df, 1x/day) (View Olmetec Review and Olmetec Label ), ACETAMINOPHEN W/ CODEINE (View Acetaminophen W/ Codeine Review and Acetaminophen W/ Codeine Label ).

6912988-5 | Hepatic Enzyme Increased
on May 11, 2009 Male patient from UNITED STATES , 71 years of age, was treated with Lopid (View Usage). Patient experienced the following unwanted or unexpected effects: hepatic enzyme increased. Lopid dosage: .


6912805-3 | Fatigue, Rhabdomyolysis
on Jan 20, 2009 Male patient from UNITED STATES , 71 years of age, was treated with Lopid (View Usage). Patient had the following side effects: fatigue, rhabdomyolysis. Lopid dosage: .

6912651-0 | Diarrhoea
Patient was taking Lopid (View Usage). After Lopid was administered, patient had the following side effects: diarrhoea on Sep 19, 2008 from UNITED STATES Additional patient health information: Male patient , weighting 198.0 lb, was diagnosed with blood triglycerides increased and. Lopid dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), LOPERAMIDE HYDROCHLORIDE (View Loperamide Hydrochloride Review and Loperamide Hydrochloride Label ), KAOPECTATE (View Kaopectate Review and Kaopectate Label ).

6912299-8 | Pruritus, Rash
Adverse event was reported on Feb 19, 2008 by a Female patient taking Lopid (View Usage) (Dosage: ) was diagnosed with blood triglycerides increased and. Location: UNITED STATES , weighting 150.4 lb, Patient experienced the following unwanted or unexpected effects: pruritus, rash (What is rash?). During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ).

6911821-5 | Colitis, Gallbladder Disorder
on Aug 08, 2007 Male patient from UNITED STATES , weighting 215.0 lb, was diagnosed with hypertriglyceridaemia and was treated with Lopid (View Usage). Patient had the following side effects: colitis, gallbladder disorder. Lopid dosage: . During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ), METOPROLOL (View Metoprolol Review and Metoprolol Label ), ACETYLSALICYLIC ACID SRT (View Acetylsalicylic Acid Srt Review and Acetylsalicylic Acid Srt Label ).

6763275-X | Diarrhoea, Pancreatitis Acute, Weight Decreased
on Jun 08, 2010 Female patient from UNITED STATES , 71 years of age, weighting 142.0 lb, was diagnosed with hyperlipidaemia, hypertriglyceridaemia and was treated with Lopid (View Usage). After Lopid was administered, patient had the following side effects: diarrhoea, pancreatitis acute, weight decreased. Lopid dosage: 600 Mg Twice Daily Po. Patient was hospitalized.

6710103-4 | Photopsia, Visual Impairment
Patient was taking Lopid (View Usage). Patient experienced the following unwanted or unexpected effects: photopsia, visual impairment on Apr 23, 2010 from COLOMBIA Additional patient health information: Male patient , 59 years of age, was diagnosed with blood triglycerides increased and. Lopid dosage: 900 Mg, 1x/day.

6688130-5 | Photopsia, Visual Impairment
Adverse event was reported on Apr 09, 2010 by a Male patient taking Lopid (View Usage) (Dosage: 900 Mg, 1x/day) was diagnosed with blood triglycerides increased and. Location: COLOMBIA , 59 years of age, Patient had the following side effects: photopsia, visual impairment.

6683919-0 | Arthralgia, Bone Pain, Muscular Weakness, Myalgia
on Apr 06, 2010 Female patient from DENMARK , 56 years of age, weighting 145.5 lb, was diagnosed with hypercholesterolaemia and was treated with Lopid (View Usage). After Lopid was administered, patient had the following side effects: arthralgia, bone pain, muscular weakness, myalgia. Lopid dosage: 600 Mg, 2x/day. During the same period patient was treated with OLBETAM (250 Mg, 3x/day) (View Olbetam Review and Olbetam Label ), ELTROXIN (50 Mg, 2x/day) (View Eltroxin Review and Eltroxin Label ).

6669173-4 | Arthralgia, Bone Pain, Muscular Weakness, Myalgia
on Mar 25, 2010 Female patient from DENMARK , 56 years of age, weighting 145.5 lb, was diagnosed with hypercholesterolaemia and was treated with Lopid (View Usage). Patient experienced the following unwanted or unexpected effects: arthralgia, bone pain, muscular weakness, myalgia. Lopid dosage: 600 Mg, 2x/day. During the same period patient was treated with OLBETAM (250 Mg, 3x/day) (View Olbetam Review and Olbetam Label ), ELTROXIN (50 Mg, 2x/day) (View Eltroxin Review and Eltroxin Label ).

6545582-9 | Erythema Multiforme
Patient was taking Lopid (View Usage). Patient had the following side effects: erythema multiforme on Jan 11, 2010 from TURKEY Additional patient health information: Male patient , 46 years of age, was diagnosed with hyperlipidaemia and. Lopid dosage: 600 Mg, 2x/day.

6312234-X | Abasia, Decreased Appetite, Diarrhoea, Metabolic Acidosis, Renal Failure Acute, Renal Tubular Necrosis, Rhabdomyolysis, Vascular Insufficiency
Adverse event was reported on Aug 13, 2009 by a Male patient taking Lopid (View Usage) (Dosage: ) . Location: UNITED STATES , 79 years of age, weighting 172.0 lb, After Lopid was administered, patient had the following side effects: abasia, decreased appetite, diarrhoea, metabolic acidosis, renal failure acute, renal tubular necrosis, rhabdomyolysis, vascular insufficiency. During the same period patient was treated with ZOCOR (80 Mg Daily Po) (View Zocor Review and Zocor Label ). Patient was hospitalized.

6294563-1 | Diplopia
on Jul 23, 2009 Female patient from SOUTH AFRICA , 48 years of age, was diagnosed with hypertriglyceridaemia and was treated with Lopid (View Usage). Patient experienced the following unwanted or unexpected effects: diplopia. Lopid dosage: Unit Dose: Unk; Frequency: Unk, Unk;.

6294344-9 | Arthritis, Decreased Appetite, Depression, Weight Decreased
on Aug 01, 2009 Female patient from UNITED STATES , weighting 125.0 lb, was diagnosed with blood cholesterol increased, blood triglycerides increased and was treated with Lopid (View Usage). Patient had the following side effects: arthritis (What is arthritis?), decreased appetite, depression (What is depression?), weight decreased. Lopid dosage: Unk. During the same period patient was treated with EFFEXOR XR (Unk) (View Effexor Xr Review and Effexor Xr Label ), LISINOPRIL (Unk) (View Lisinopril Review and Lisinopril Label ), CARDIZEM (Unk) (View Cardizem Review and Cardizem Label ), ATENOLOL (Unk) (View Atenolol Review and Atenolol Label ), LAMICTAL (Unk) (View Lamictal Review and Lamictal Label ).

6246748-8 | Arthritis, Decreased Appetite, Depression, Weight Decreased
Patient was taking Lopid (View Usage). After Lopid was administered, patient had the following side effects: arthritis (What is arthritis?), decreased appetite, depression (What is depression?), weight decreased on Jun 16, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 125.0 lb, was diagnosed with blood cholesterol increased, blood triglycerides increased and. Lopid dosage: Unk. During the same period patient was treated with EFFEXOR XR (Unk) (View Effexor Xr Review and Effexor Xr Label ), LISINOPRIL (Unk) (View Lisinopril Review and Lisinopril Label ), CARDIZEM (Unk) (View Cardizem Review and Cardizem Label ), ATENOLOL (Unk) (View Atenolol Review and Atenolol Label ), LAMICTAL (Unk) (View Lamictal Review and Lamictal Label ).

6187710-3 | Renal Failure Acute
Adverse event was reported on Apr 30, 2009 by a Female patient taking Lopid (View Usage) (Dosage: 600 Mg, 2x/day) was diagnosed with hypercholesterolaemia and. Location: DENMARK , 68 years of age, Patient experienced the following unwanted or unexpected effects: renal failure acute. Patient was hospitalized.

5844097-0 | Anger, Disturbance In Attention, Insomnia, Mood Swings
on Aug 04, 2008 Female patient from IRELAND , weighting 210.1 lb, was treated with Lopid (View Usage). Patient had the following side effects: anger, disturbance in attention, insomnia, mood swings. Lopid dosage: .

5840884-3 | Neutropenia, White Blood Cell Count Decreased
on Jul 30, 2008 Male patient from UNITED STATES , weighting 169.1 lb, was diagnosed with hyperlipidaemia and was treated with Lopid (View Usage). After Lopid was administered, patient had the following side effects: neutropenia, white blood cell count decreased. Lopid dosage: . During the same period patient was treated with ARICEPT (View Aricept Review and Aricept Label ), DETROL (View Detrol Review and Detrol Label ), GLYBURIDE (View Glyburide Review and Glyburide Label ), LIPITOR (View Lipitor Review and Lipitor Label ), PROTONIX (View Protonix Review and Protonix Label ), CALCIUM (View Calcium Review and Calcium Label ), VITAMIN D (View Vitamin D Review and Vitamin D Label ).

5824995-4 | Blood Cholesterol Increased, Low Density Lipoprotein Increased, Red Blood Cell Sedimentation Rate Increased, Rheumatoid Factor Increased
Patient was taking Lopid (View Usage). Patient experienced the following unwanted or unexpected effects: blood cholesterol increased, low density lipoprotein increased, red blood cell sedimentation rate increased, rheumatoid factor increased on Jul 16, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 214.3 lb, was diagnosed with hypertriglyceridaemia and. Lopid dosage: . During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), FAMOTIDINE (View Famotidine Review and Famotidine Label ), ATIVAN (View Ativan Review and Ativan Label ).

5739478-X | Choluria, Headache, Hepatic Function Abnormal, Nausea, Pyrexia
Adverse event was reported on May 07, 2008 by a Female patient taking Lopid (View Usage) (Dosage: 600mg Daily) was diagnosed with herpes zoster and. Location: AUSTRALIA , 59 years of age, weighting 172.0 lb, Patient had the following side effects: choluria, headache (What is headache?), hepatic function abnormal, nausea (What is nausea?), pyrexia. During the same period patient was treated with OGEN (1.2mg Daily) (View Ogen Review and Ogen Label ), PROVERA (5mg Daily) (View Provera Review and Provera Label ), LOSEC /SWE/ (20mg Daily) (View Losec /swe/ Review and Losec /swe/ Label ), FAMVIR (750mg Daily) (View Famvir Review and Famvir Label ).

5713356-4 | Cellulitis, Face Oedema, Myalgia, Pyrexia, Urticaria
on Apr 11, 2008 Female patient from UNITED STATES , weighting 190.4 lb, was diagnosed with blood triglycerides increased, cellulitis (What is cellulitis?), hypothyroidism and was treated with Lopid (View Usage). After Lopid was administered, patient had the following side effects: cellulitis (What is cellulitis?), face oedema, myalgia, pyrexia, urticaria. Lopid dosage: Daily Dose:600mg-freq:daily. During the same period patient was treated with AVELOX (Daily Dose:400mg-freq:daily) (View Avelox Review and Avelox Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ).

5679539-7 | Cellulitis, Face Oedema, Myalgia, Pyrexia, Urticaria
on Mar 13, 2008 Female patient from UNITED STATES , weighting 190.4 lb, was diagnosed with blood triglycerides increased, cellulitis (What is cellulitis?) and was treated with Lopid (View Usage). Patient experienced the following unwanted or unexpected effects: cellulitis (What is cellulitis?), face oedema, myalgia, pyrexia, urticaria. Lopid dosage: Daily Dose:600mg-text:600 Mg-freq:daily. During the same period patient was treated with AVELOX (Daily Dose:400mg-text:400 Mg-freq:daily) (View Avelox Review and Avelox Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ).

5599359-1 | Arteriosclerosis, Cholelithiasis, Cystocele, Musculoskeletal Pain, Myalgia, Stomach Discomfort, Synovial Cyst
Patient was taking Lopid (View Usage). Patient had the following side effects: arteriosclerosis, cholelithiasis, cystocele, musculoskeletal pain, myalgia, stomach discomfort, synovial cyst on Jan 10, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 213.0 lb, was diagnosed with blood cholesterol increased, blood triglycerides increased and. Lopid dosage: . During the same period patient was treated with FUROSEMIDE (View Furosemide Review and Furosemide Label ), VITAMIN CAP (View Vitamin Cap Review and Vitamin Cap Label ), CALCIUM WITH VITAMIN D (View Calcium With Vitamin D Review and Calcium With Vitamin D Label ), ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid Label ), VITAMIN E (View Vitamin E Review and Vitamin E Label ), GLUCOSAMINE (View Glucosamine Review and Glucosamine Label ).

5573796-3 | Abdominal Pain, Diarrhoea, Dyspepsia, Haematochezia, Nausea
Adverse event was reported on Dec 17, 2007 by a Male patient taking Lopid (View Usage) (Dosage: ) . Location: PORTUGAL , weighting 176.4 lb, After Lopid was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), diarrhoea, dyspepsia, haematochezia, nausea (What is nausea?). During the same period patient was treated with BISOPROLOL FUMARATE (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ), VALSARTAN (View Valsartan Review and Valsartan Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

5555943-2 | Abdominal Pain, Diarrhoea, Dyspepsia, Haematochezia, Nausea
on Dec 03, 2007 Male patient from PORTUGAL , weighting 176.4 lb, was treated with Lopid (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), diarrhoea, dyspepsia, haematochezia, nausea (What is nausea?). Lopid dosage: . During the same period patient was treated with BISOPROLOL FUMARATE (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ), VALSARTAN (View Valsartan Review and Valsartan Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

5502492-3 | Abdominal Pain, Diarrhoea, Dyspepsia, Haematochezia, Nausea
on Oct 19, 2007 Male patient from PORTUGAL , weighting 176.4 lb, was treated with Lopid (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), diarrhoea, dyspepsia, haematochezia, nausea (What is nausea?). Lopid dosage: . During the same period patient was treated with BISOPROLOL FUMARATE (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ), VALSARTAN (View Valsartan Review and Valsartan Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

5487461-4 | Movement Disorder, Myalgia
Patient was taking Lopid (View Usage). After Lopid was administered, patient had the following side effects: movement disorder (What is movement disorder?), myalgia on Oct 04, 2007 from PORTUGAL Additional patient health information: Female patient , 85 years of age, weighting 110.2 lb, was diagnosed with hypercholesterolaemia and. Lopid dosage: Daily Dose:600mg-text:600 Mg Daily. During the same period patient was treated with PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ).

5483548-0 | Breakthrough Pain, Condition Aggravated, Loss Of Employment, Muscle Disorder, Muscular Weakness, Myalgia, Pain In Extremity
Adverse event was reported on Oct 10, 2007 by a Female patient taking Lopid (View Usage) (Dosage: 600 Mg 2xs Daily) was diagnosed with blood cholesterol increased and. Location: UNITED STATES , 38 years of age, weighting 180.0 lb, Patient experienced the following unwanted or unexpected effects: breakthrough pain, condition aggravated, loss of employment, muscle disorder (What is muscle disorder?), muscular weakness, myalgia, pain in extremity.

5482773-2 | Balance Disorder, Muscle Spasms, Muscle Strain, Pneumonia, Renal Artery Stenosis, Skin Disorder, Skin Wrinkling, Stomach Discomfort, Weight Decreased
on Sep 28, 2007 Female patient from UNITED STATES , weighting 113.2 lb, was diagnosed with blood triglycerides increased, blood cholesterol increased and was treated with Lopid (View Usage). Patient had the following side effects: balance disorder, muscle spasms, muscle strain, pneumonia (What is pneumonia?), renal artery stenosis, skin disorder, skin wrinkling, stomach discomfort, weight decreased. Lopid dosage: . During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), GLIMEPIRIDE (View Glimepiride Review and Glimepiride Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ).

5475512-2 | Anorexia, Blood Pressure Abnormal, Depression, Insomnia
on Jul 10, 2007 Male patient from UNITED STATES , 46 years of age, weighting 200.4 lb, was diagnosed with blood cholesterol increased, pain (What is pain?) and was treated with Lopid (View Usage). After Lopid was administered, patient had the following side effects: anorexia, blood pressure abnormal, depression (What is depression?), insomnia. Lopid dosage: 600 Mg Twice Daily. During the same period patient was treated with LORTAB (View Lortab Review and Lortab Label ), HYDROCODONE BITARTRATE (View Hydrocodone Bitartrate Review and Hydrocodone Bitartrate Label ).

5424159-2 | Movement Disorder, Myalgia
Patient was taking Lopid (View Usage). Patient experienced the following unwanted or unexpected effects: movement disorder (What is movement disorder?), myalgia on Aug 13, 2007 from PORTUGAL Additional patient health information: Female patient , 85 years of age, weighting 110.2 lb, was diagnosed with hypercholesterolaemia and. Lopid dosage: Daily Dose:600mg-text:600 Mg Daily. During the same period patient was treated with PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ).

5408911-5 | Penile Discharge, Urinary Tract Infection
Adverse event was reported on Jul 27, 2007 by a Male patient taking Lopid (View Usage) (Dosage: ) was diagnosed with hypertriglyceridaemia and. Location: BRAZIL , weighting 187.4 lb, Patient had the following side effects: penile discharge, urinary tract infection (What is urinary tract infection?).

5354865-X | Blood Glucose Increased
on Jun 04, 2007 Male patient from AUSTRALIA , weighting 218.3 lb, was diagnosed with blood triglycerides increased and was treated with Lopid (View Usage). After Lopid was administered, patient had the following side effects: blood glucose increased. Lopid dosage: . During the same period patient was treated with AVAPRO (View Avapro Review and Avapro Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), DIAMICRON (View Diamicron Review and Diamicron Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), LANTUS (Text:40 Units-freq:at Night) (View Lantus Review and Lantus Label ), PRAZOSIN HCL (View Prazosin Hcl Review and Prazosin Hcl Label ).

5342458-X | Chest Discomfort, Dyspnoea, Pharyngeal Oedema, Suffocation Feeling, Weight Increased
on May 21, 2007 Female patient from UNITED STATES , weighting 170.0 lb, was diagnosed with blood cholesterol increased, blood triglycerides increased and was treated with Lopid (View Usage). Patient experienced the following unwanted or unexpected effects: chest discomfort, dyspnoea, pharyngeal oedema, suffocation feeling, weight increased. Lopid dosage: . During the same period patient was treated with LIDODERM (View Lidoderm Review and Lidoderm Label ), DURAGESIC 100 (View Duragesic-100 Review and Duragesic-100 Label ), SPIRIVA (View Spiriva Review and Spiriva Label ), FLOVENT (View Flovent Review and Flovent Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), PRILOSEC (View Prilosec Review and Prilosec Label ), ERYTHROMYCIN (View Erythromycin Review and Erythromycin Label ).

5318177-2 | Asthenia, Blood Creatinine Decreased, Muscle Atrophy, Muscular Weakness, Pain, Pyrexia
Patient was taking Lopid (View Usage). Patient had the following side effects: asthenia, blood creatinine decreased, muscle atrophy, muscular weakness, pain (What is pain?), pyrexia on Apr 25, 2007 from UNITED STATES Additional patient health information: Male patient , weighting 200.0 lb, was diagnosed with blood triglycerides increased and. Lopid dosage: . During the same period patient was treated with LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ).

5280124-X | Myalgia
Adverse event was reported on Mar 27, 2007 by a Male patient taking Lopid (View Usage) (Dosage: ) . Location: UNITED STATES , 59 years of age, weighting 291.9 lb, After Lopid was administered, patient had the following side effects: myalgia.

5280064-6 | Rash
on Mar 27, 2007 Male patient from UNITED STATES , 69 years of age, weighting 207.0 lb, was treated with Lopid (View Usage). Patient experienced the following unwanted or unexpected effects: rash (What is rash?). Lopid dosage: .

5270291-6 | Hyperlipidaemia, Leukocytosis, Liver Disorder, Malaise, Myositis, Nephrotic Syndrome, Platelet Count Increased, Rhabdomyolysis, Viral Infection
on Mar 08, 2007 Male patient from COLOMBIA , 42 years of age, was diagnosed with dyslipidaemia and was treated with Lopid (View Usage). Patient had the following side effects: hyperlipidaemia, leukocytosis, liver disorder, malaise, myositis (What is myositis?), nephrotic syndrome, platelet count increased, rhabdomyolysis, viral infection (What is viral infection?). Lopid dosage: . During the same period patient was treated with LIPOBAY (Daily Dose:.4mg) (View Lipobay Review and Lipobay Label ), METICORTEN (View Meticorten Review and Meticorten Label ), CLOFIBRATE (View Clofibrate Review and Clofibrate Label ). Patient was hospitalized.

5254624-2 | Asthenia, Blood Creatinine Decreased, Muscle Atrophy, Muscular Weakness, Pain, Pyrexia
Patient was taking Lopid (View Usage). After Lopid was administered, patient had the following side effects: asthenia, blood creatinine decreased, muscle atrophy, muscular weakness, pain (What is pain?), pyrexia on Feb 20, 2007 from UNITED STATES Additional patient health information: Male patient , weighting 200.0 lb, was diagnosed with blood triglycerides increased and. Lopid dosage: . During the same period patient was treated with LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ).

5254448-6 | Hyperlipidaemia, Leukocytosis, Liver Disorder, Malaise, Myositis, Nephrotic Syndrome, Platelet Count Increased, Rhabdomyolysis, Viral Infection
Adverse event was reported on Feb 20, 2007 by a Male patient taking Lopid (View Usage) (Dosage: ) was diagnosed with dyslipidaemia and. Location: COLOMBIA , 42 years of age, Patient experienced the following unwanted or unexpected effects: hyperlipidaemia, leukocytosis, liver disorder, malaise, myositis (What is myositis?), nephrotic syndrome, platelet count increased, rhabdomyolysis, viral infection (What is viral infection?). During the same period patient was treated with LIPOBAY (View Lipobay Review and Lipobay Label ), METICORTEN (View Meticorten Review and Meticorten Label ), CLOFIBRATE (View Clofibrate Review and Clofibrate Label ). Patient was hospitalized.

5188735-7 | Chest Discomfort, Dyspnoea, Oropharyngeal Swelling
on Dec 01, 2006 Female patient from UNITED STATES , 47 years of age, weighting 170.0 lb, was diagnosed with blood cholesterol increased, blood triglycerides increased and was treated with Lopid (View Usage). Patient had the following side effects: chest discomfort, dyspnoea, oropharyngeal swelling. Lopid dosage: 1200 Mg (600 Mg, 2 In 1 D). During the same period patient was treated with LIDODERM PATCH (LIDOCAINE HYDROCHLORIDE) (View Lidoderm Patch (lidocaine Hydrochloride) Review and Lidoderm Patch (lidocaine Hydrochloride) Label ), DURAGESIC 100 (View Duragesic-100 Review and Duragesic-100 Label ), SPIRIVA (View Spiriva Review and Spiriva Label ), FLOVENT (View Flovent Review and Flovent Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), PRILOSEC (View Prilosec Review and Prilosec Label ), ERYTHROMYCIN (View Erythromycin Review and Erythromycin Label ).

5145768-4 | Blood Creatine Phosphokinase Increased, C-reactive Protein, Musculoskeletal Discomfort, Red Blood Cell Sedimentation Rate Increased, Restless Legs Syndrome
on Jun 19, 2006 Male patient from UNITED STATES , 39 years of age, weighting 274.0 lb, was diagnosed with blood cholesterol increased, blood triglycerides and was treated with Lopid (View Usage). After Lopid was administered, patient had the following side effects: blood creatine phosphokinase increased, c-reactive protein, musculoskeletal discomfort, red blood cell sedimentation rate increased, restless legs syndrome. Lopid dosage: 1200 Mg (600 Mg,2 In 1 D).

5144258-2 | Swollen Tongue
Patient was taking Lopid (View Usage). Patient experienced the following unwanted or unexpected effects: swollen tongue on Nov 02, 2006 from UNITED STATES Additional patient health information: Male patient , 67 years of age, weighting 218.0 lb, was diagnosed with hypertriglyceridaemia and. Lopid dosage: 600mg Bid Po.

5131802-4 | Hepatic Steatosis
Adverse event was reported on Oct 04, 2006 by a Male patient taking Lopid (View Usage) (Dosage: 900 Mg, Oral) was diagnosed with blood triglycerides increased and. Location: ARGENTINA , 39 years of age, Patient had the following side effects: hepatic steatosis. During the same period patient was treated with AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), HYDROCHOROTHIAZIDE (HYDROCHLOROTHIAZIDE) (View Hydrochorothiazide (hydrochlorothiazide) Review and Hydrochorothiazide (hydrochlorothiazide) Label ).

5091893-6 | Gait Disturbance, Tendon Disorder, Tendon Rupture
on Aug 16, 2006 Female patient from UNITED KINGDOM , 74 years of age, was treated with Lopid (View Usage). After Lopid was administered, patient had the following side effects: gait disturbance, tendon disorder, tendon rupture. Lopid dosage: 1200 Mg (600 Mg, 2 In 1 D). During the same period patient was treated with ARTHROTEC (View Arthrotec Review and Arthrotec Label ), CALCHICHEW (CALCIUM CARBONATE) (View Calchichew (calcium Carbonate) Review and Calchichew (calcium Carbonate) Label ).

5086172-7 | Gait Disturbance, Tendon Rupture
on Aug 07, 2006 Female patient from UNITED KINGDOM , 74 years of age, was treated with Lopid (View Usage). Patient experienced the following unwanted or unexpected effects: gait disturbance, tendon rupture. Lopid dosage: .

5009737-7 | Incorrect Dose Administered, Suicide Attempt, Vomiting
Patient was taking Lopid (View Usage). Patient had the following side effects: incorrect dose administered, suicide attempt, vomiting on May 11, 2006 from PHILIPPINES Additional patient health information: Female patient , 19 years of age, was diagnosed with ill-defined disorder and. Lopid dosage: Oral. Patient was hospitalized.

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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 Lopid 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 Lopid quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Lopid 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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Lopid Reactions
Abdominal PainWhat is Abdominal pain?
Anaemia
AnxietyWhat is Anxiety?
Arthralgia
ArthritisWhat is Arthritis?
Asthenia
Blood Creatine Phosphokinase Increased
Blood Creatinine Decreased
Blood Glucose Increased
Blood Test Abnormal
Bone Pain
Decreased Appetite
DepressionWhat is Depression?
Diarrhoea
Dyspepsia
Dyspnoea
Haematochezia
Libido Decreased
Malaise
Muscular Weakness
Myalgia
MyositisWhat is Myositis?
NauseaWhat is Nausea?
PainWhat is Pain?
Pyrexia
Renal Failure Acute
Rhabdomyolysis
Stomach Discomfort
Vomiting
Weight Decreased
Lopid 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 Lopid 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!