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I USE RENITEC 20mg tabs and take other medication elltroxin, glucophage These tablets are ...Keep Reading

dose novothral 75 mg, euthroyrox 50 mg and glucophage 1000 cause uterine bleeding ...Keep Reading

dose novothral 75 mg, euthroyrox 50 mg and glucophage 1000 cause uterine bleeding ...Keep Reading

Tried Januvia. Loved it. Brought my BS to normal limits immediately, ...Keep Reading

i am hypertensive, type 2 diabetic mellitus, hyperlipidemia. i am using ...Keep Reading

Reading about all the horrendous side effects some of which i am experiencing myself ...Keep Reading

I am currently on the following medication after an Heart Attack 7 years ago....Keep Reading

I have been onto Januvia for the last year and half and have been ...Keep Reading

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Dizziness, Coma, TI (1)
Gout (1)
Rash (1)
Vertigo (1)
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Common Glucophage Side Effects

top 5 Glucophage|Dizziness,|Gout|Rash|Vertigo adverse effects>>See All Glucophage Side Effects

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Glucophage adverse events reported to FDA.

Have You Experienced unusual Glucophage symptoms? PatientsVille.com collects and analyzes Glucophage side effect and adverse reports submitted by Glucophage users, such as musculo skeletal pains in the chest ,two|AFFECTING FACIAL SKIN LIKE ECSUMA,ITCHING AND SMALL|diarrhoea, headaches, naseated feeling |nausea, diarrhoea, vomiting, photophobia, night sweats |.

Summary

FDA Adverse Reports: 1177. View All

Glucophage FDA safety alerts: No

Reported deaths: 151

Reported hospitalizations: 516

Glucophage Dosage, Warnings, Usage.

Post Your Unusual Symptoms:

Most Reported
1Gout
2Dizziness, Coma, TI
3Rash
4Vertigo
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Recent Drug Reports

musculo skeletal pains in the chest ,two

AFFECTING FACIAL SKIN LIKE ECSUMA,ITCHING AND SMALL

diarrhoea, headaches, naseated feeling

nausea, diarrhoea, vomiting, photophobia, night sweats

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

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Showing 1-50 of 1177  Next Page  >

7002459-2 | Abnormal Behaviour, Confusional State, Diarrhoea, Haematoma, Lactic Acidosis, Renal Failure, Septic Shock, Vomiting
on Sep 10, 2010 Female patient from GERMANY , 67 years of age, was diagnosed with diabetes mellitus and was treated with Glucophage (View Usage). Patient experienced the following unwanted or unexpected effects: abnormal behaviour, confusional state, diarrhoea, haematoma, lactic acidosis, renal failure, septic shock, vomiting. Glucophage dosage: . Patient was hospitalized.

6985608-1 | Hypoglycaemia, Loss Of Consciousness
Patient was taking Glucophage (View Usage). Patient had the following side effects: hypoglycaemia, loss of consciousness on Sep 07, 2010 from GERMANY Additional patient health information: Male patient , 57 years of age, was diagnosed with diabetes mellitus and. Glucophage dosage: . During the same period patient was treated with LEVEMIR (View Levemir Review and Levemir Label ), NOVORAPID (View Novorapid Review and Novorapid Label ), TICLOPIDINE HCL (View Ticlopidine Hcl Review and Ticlopidine Hcl Label ), LYRICA (View Lyrica Review and Lyrica Label ), CONGESCOR (View Congescor Review and Congescor Label ), TAREG (View Tareg Review and Tareg Label ), PRILOSEC (View Prilosec Review and Prilosec Label ), NORVASC (View Norvasc Review and Norvasc Label ).

6973493-3 | Pulmonary Mass, Stent Placement
Adverse event was reported on Sep 07, 2010 by a Female patient taking Glucophage (View Usage) (Dosage: Taken For 18yrs) . Location: UNITED STATES , 75 years of age, weighting 158.7 lb, After Glucophage was administered, patient had the following side effects: pulmonary mass, stent placement. During the same period patient was treated with GLUCOTROL XL (View Glucotrol Xl Review and Glucotrol Xl Label ), JANUVIA (View Januvia Review and Januvia Label ), AVAPRO (Started 10 Yrs Age) (View Avapro Review and Avapro Label ), THYROID SUPPLEMENT (View Thyroid Supplement Review and Thyroid Supplement Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LIPITOR (View Lipitor Review and Lipitor Label ), NEURONTIN (View Neurontin Review and Neurontin Label ). Patient was hospitalized.

6969087-6 | Pancreatitis
on Aug 26, 2010 Male patient from GERMANY , 55 years of age, was treated with Glucophage (View Usage). Patient experienced the following unwanted or unexpected effects: pancreatitis. Glucophage dosage: . During the same period patient was treated with BYETTA (10mg Bid:may2010 To 30may2010 Soln For Inj) (View Byetta Review and Byetta Label ), CRESTOR (Tablet) (View Crestor Review and Crestor Label ), PLAVIX (Tablet) (View Plavix Review and Plavix Label ), TRIATEC (Tablet) (View Triatec Review and Triatec Label ), NOVONORM (View Novonorm Review and Novonorm Label ), CELESTONE (View Celestone Review and Celestone Label ), OROCAL (View Orocal Review and Orocal Label ). Patient was hospitalized.


6966947-7 | Renal Failure
on Aug 26, 2010 Male patient from GERMANY , 65 years of age, was diagnosed with type 2 diabetes mellitus, renal hypertension and was treated with Glucophage (View Usage). Patient had the following side effects: renal failure. Glucophage dosage: Glucophage 1000mg. During the same period patient was treated with BYETTA (Byetta 5mcg Soln For Inj) (View Byetta Review and Byetta Label ), ENALAPRIL MALEATE (1df= 20mg Tab) (View Enalapril Maleate Review and Enalapril Maleate Label ), IPERTEN (Tabs 1df=20mg) (View Iperten Review and Iperten Label ), APROVEL (Tabs 1df=300mg) (View Aprovel Review and Aprovel Label ), KERLONE (Coated Tablet) (View Kerlone Review and Kerlone Label ), LASIX (1df=120mg) (View Lasix Review and Lasix Label ), REGULAR INSULIN (View Regular Insulin Review and Regular Insulin Label ). Patient was hospitalized.

6958020-9 | Diarrhoea, Lactic Acidosis, Renal Failure Acute, Shock, Vomiting
Patient was taking Glucophage (View Usage). After Glucophage was administered, patient had the following side effects: diarrhoea, lactic acidosis, renal failure acute, shock, vomiting on Aug 23, 2010 from GERMANY Additional patient health information: Female patient , 46 years of age, was diagnosed with type 2 diabetes mellitus and. Glucophage dosage: . During the same period patient was treated with VICTOZA (1df=6mg/ml Soln For Inj) (View Victoza Review and Victoza Label ), ACTRAPID (View Actrapid Review and Actrapid Label ), INSULATARD (Injection) (View Insulatard Review and Insulatard Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), LOGIMAX (Prolonged Release Ablet) (View Logimax Review and Logimax Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), VALSARTAN AND HYDROCHLOROTHIAZIDE (Tab) (View Valsartan And Hydrochlorothiazide Review and Valsartan And Hydrochlorothiazide Label ), KARDEGIC (Powder + Solvent For Oral Solution) (View Kardegic Review and Kardegic Label ). Patient was hospitalized.

6958017-9 | Hepatic Steatosis
Adverse event was reported on Aug 17, 2010 by a Female patient taking Glucophage (View Usage) (Dosage: ) was diagnosed with type 2 diabetes mellitus and. Location: GERMANY , 54 years of age, Patient experienced the following unwanted or unexpected effects: hepatic steatosis.

6925256-2 | Transitional Cell Carcinoma
on Aug 11, 2010 Male patient from UNITED STATES , 68 years of age, weighting 174.2 lb, was diagnosed with diabetes mellitus and was treated with Glucophage (View Usage). Patient had the following side effects: transitional cell carcinoma. Glucophage dosage: Using For 3 Plus Yrs (2007-2010).. During the same period patient was treated with AMARYL (View Amaryl Review and Amaryl Label ). Patient was hospitalized.

6922864-X | Hepatitis
on Aug 03, 2010 Male patient from GERMANY , 55 years of age, was diagnosed with diabetes mellitus and was treated with Glucophage (View Usage). After Glucophage was administered, patient had the following side effects: hepatitis (What is hepatitis?). Glucophage dosage: Glucophage Xr 1000mg. During the same period patient was treated with FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), PIOGLITAZONE HCL (View Pioglitazone Hcl Review and Pioglitazone Hcl Label ), NATEGLINIDE (View Nateglinide Review and Nateglinide Label ), LIPITOR (View Lipitor Review and Lipitor Label ).

6922795-5 | Erythema, Hyperglycaemia, Pruritus, Urticaria
Patient was taking Glucophage (View Usage). Patient experienced the following unwanted or unexpected effects: erythema, hyperglycaemia, pruritus, urticaria on Aug 02, 2010 from GERMANY Additional patient health information: Female patient , 65 years of age, was diagnosed with type 2 diabetes mellitus and. Glucophage dosage: 1700mg/day. During the same period patient was treated with METFORMIN HCL (1700mg/day) (View Metformin Hcl Review and Metformin Hcl Label ), GLIBENCLAMIDE (View Glibenclamide Review and Glibenclamide Label ), ENALAPRIL (View Enalapril Review and Enalapril Label ), INDAPAMIDE (View Indapamide Review and Indapamide Label ), BETAHISTINE (View Betahistine Review and Betahistine Label ).

6922729-3 | Haematuria, Lactic Acidosis, Urinary Retention, Urinary Tract Infection
Adverse event was reported on Jul 26, 2010 by a Male patient taking Glucophage (View Usage) (Dosage: Film Coated Tablet) was diagnosed with diabetes mellitus and. Location: GERMANY , 73 years of age, Patient had the following side effects: haematuria, lactic acidosis, urinary retention, urinary tract infection (What is urinary tract infection?). During the same period patient was treated with COZAAR (Film Coated Tablet) (View Cozaar Review and Cozaar Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), FINASTERIDE (View Finasteride Review and Finasteride Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), ACETAMINOPHEN (Film Coated Tablet) (View Acetaminophen Review and Acetaminophen Label ), BETAPRED (Tab) (View Betapred Review and Betapred Label ), BEHEPAN (Film Coated Tablet) (View Behepan Review and Behepan Label ). Patient was hospitalized.

6912488-2 | Off Label Use, Toxic Epidermal Necrolysis
on Jul 22, 2010 Female patient from GERMANY , 48 years of age, was diagnosed with type 2 diabetes mellitus, arthralgia and was treated with Glucophage (View Usage). After Glucophage was administered, patient had the following side effects: off label use, toxic epidermal necrolysis. Glucophage dosage: . During the same period patient was treated with TEGRETOL (View Tegretol Review and Tegretol Label ). Patient was hospitalized.

6910483-0 | Nephrectomy
on Aug 03, 2010 Male patient from UNITED STATES , 68 years of age, weighting 174.2 lb, was treated with Glucophage (View Usage). Patient experienced the following unwanted or unexpected effects: nephrectomy. Glucophage dosage: . During the same period patient was treated with AMARYL (View Amaryl Review and Amaryl Label ). Patient was hospitalized.

6895639-8 | Asthenia, Back Pain, Diarrhoea, Hyperkalaemia, International Normalised Ratio Increased, Lactic Acidosis, Renal Failure Acute, Vomiting
Patient was taking Glucophage (View Usage). Patient had the following side effects: asthenia, back pain (What is back pain?), diarrhoea, hyperkalaemia, international normalised ratio increased, lactic acidosis, renal failure acute, vomiting on Jul 22, 2010 from GERMANY Additional patient health information: Male patient , 84 years of age, was diagnosed with type 2 diabetes mellitus and. Glucophage dosage: . During the same period patient was treated with VASTAREL (View Vastarel Review and Vastarel Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), DIAMICRON (View Diamicron Review and Diamicron Label ), SERC (View Serc Review and Serc Label ), OMIX (View Omix Review and Omix Label ), PERMIXON (View Permixon Review and Permixon Label ), BISOPROLOL FUMARATE (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), PREVISCAN (View Previscan Review and Previscan Label ). Patient was hospitalized.

6895471-5 | Decreased Appetite, Dehydration, Diarrhoea, Hypoglycaemia, Lactic Acidosis, Renal Failure Acute, Vomiting
Adverse event was reported on Jul 23, 2010 by a Female patient taking Glucophage (View Usage) (Dosage: ) was diagnosed with gout (What is gout?) and. Location: GERMANY , 84 years of age, After Glucophage was administered, patient had the following side effects: decreased appetite, dehydration, diarrhoea, hypoglycaemia, lactic acidosis, renal failure acute, vomiting. During the same period patient was treated with COKENZEN (View Cokenzen Review and Cokenzen Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ), DIAMICRON (View Diamicron Review and Diamicron Label ), XELEVIA (View Xelevia Review and Xelevia Label ), COLCHIMAX (View Colchimax Review and Colchimax Label ), ZYLORIC (View Zyloric Review and Zyloric Label ). Patient was hospitalized.

6894741-4 | Diarrhoea Haemorrhagic
on Jul 30, 2010 Female patient from UNITED STATES , 58 years of age, weighting 320.0 lb, was diagnosed with blood glucose increased and was treated with Glucophage (View Usage). Patient experienced the following unwanted or unexpected effects: diarrhoea haemorrhagic. Glucophage dosage: 500mg Tablet 2xday Mouth.

6894677-9 | Escherichia Sepsis, Lactic Acidosis, Pyelonephritis, Renal Cell Carcinoma
on Jul 22, 2010 Male patient from GERMANY , 62 years of age, was diagnosed with type 2 diabetes mellitus, hiv infection (What is hiv infection?) and was treated with Glucophage (View Usage). Patient had the following side effects: escherichia sepsis, lactic acidosis, pyelonephritis, renal cell carcinoma. Glucophage dosage: . During the same period patient was treated with SUSTIVA (View Sustiva Review and Sustiva Label ), ABACAVIR SULFATE AND LAMIVUDINE (1 Df=600mg/300mg Tablet) (View Abacavir Sulfate And Lamivudine Review and Abacavir Sulfate And Lamivudine Label ). Patient was hospitalized.

6894674-3 | Confusional State, Disorientation, Hypoglycaemia, Somnolence
Patient was taking Glucophage (View Usage). After Glucophage was administered, patient had the following side effects: confusional state, disorientation, hypoglycaemia, somnolence on Jul 22, 2010 from GERMANY Additional patient health information: Female patient , 74 years of age, . Glucophage dosage: . During the same period patient was treated with GLYBURIDE (View Glyburide Review and Glyburide Label ). Patient was hospitalized.

6887013-5 | Ear Infection, Transaminases Increased
Adverse event was reported on Jul 19, 2010 by a Male patient taking Glucophage (View Usage) (Dosage: ) . Location: GERMANY , 38 years of age, Patient experienced the following unwanted or unexpected effects: ear infection (What is ear infection?), transaminases increased. During the same period patient was treated with AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ), WELLVONE (View Wellvone Review and Wellvone Label ), BACTRIM (On 27nov2009 Bactrim Was Replaced By Wellvone) (View Bactrim Review and Bactrim Label ), OFLOCET (View Oflocet Review and Oflocet Label ), ABACAVIR SULFATE (View Abacavir Sulfate Review and Abacavir Sulfate Label ), ZIDOVUDINE (View Zidovudine Review and Zidovudine Label ), LAMIVUDINE (View Lamivudine Review and Lamivudine Label ). Patient was hospitalized.

6887007-X | Blood Creatine Phosphokinase Increased, Lactic Acidosis, Musculoskeletal Pain, Pyrexia, Renal Failure Acute
on Jul 19, 2010 Male patient from GERMANY , 38 years of age, was treated with Glucophage (View Usage). Patient had the following side effects: blood creatine phosphokinase increased, lactic acidosis, musculoskeletal pain, pyrexia, renal failure acute. Glucophage dosage: . During the same period patient was treated with BACTRIM (View Bactrim Review and Bactrim Label ), TRIZIVIR (View Trizivir Review and Trizivir Label ), ZIDOVUDINE (View Zidovudine Review and Zidovudine Label ), LAMIVUDINE (View Lamivudine Review and Lamivudine Label ), KALETRA TABS 200 MG/50 MG (1 Df=200/50mg) (View Kaletra Tabs 200 Mg/50 Mg Review and Kaletra Tabs 200 Mg/50 Mg Label ). Patient was hospitalized.

6883874-4 | Abortion Spontaneous, Pregnancy
on Jul 28, 2010 Female patient from CHINA , 37 years of age, was diagnosed with polycystic ovaries and was treated with Glucophage (View Usage). After Glucophage was administered, patient had the following side effects: abortion spontaneous, pregnancy (What is pregnancy?). Glucophage dosage: .

6883829-X | Abdominal Discomfort, Convulsion, Fall, Glycosylated Haemoglobin Increased, Nausea, Nervousness, Tooth Loss, Tremor
Patient was taking Glucophage (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal discomfort, convulsion, fall (What is fall?), glycosylated haemoglobin increased, nausea (What is nausea?), nervousness, tooth loss, tremor on Jul 23, 2010 from UNITED STATES Additional patient health information: Male patient , 46 years of age, . Glucophage dosage: . During the same period patient was treated with ACTOS (View Actos Review and Actos Label ), PRILOSEC (View Prilosec Review and Prilosec Label ). Patient was hospitalized.

6882424-6 | Diarrhoea, Hypoglycaemia, Lactic Acidosis, Renal Failure, Tachypnoea, Vomiting
Adverse event was reported on Jul 19, 2010 by a Male patient taking Glucophage (View Usage) (Dosage: ) was diagnosed with type 2 diabetes mellitus and. Location: GERMANY , 74 years of age, Patient had the following side effects: diarrhoea, hypoglycaemia, lactic acidosis, renal failure, tachypnoea, vomiting. During the same period patient was treated with REPAGLINIDE (1df=3u.1000mg) (View Repaglinide Review and Repaglinide Label ), TAMSULOSIN HCL (View Tamsulosin Hcl Review and Tamsulosin Hcl Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), OLPRESS (View Olpress Review and Olpress Label ), LOBIVON (View Lobivon Review and Lobivon Label ), LASIX (View Lasix Review and Lasix Label ). Patient was hospitalized.

6879810-7 | Dermatitis Bullous
on Jul 15, 2010 Male patient from GERMANY , 54 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Glucophage (View Usage). After Glucophage was administered, patient had the following side effects: dermatitis bullous. Glucophage dosage: . During the same period patient was treated with EXFORGE (View Exforge Review and Exforge Label ). Patient was hospitalized.

6870943-8 | Cardiogenic Shock, Dehydration, Diarrhoea, Lactic Acidosis, Pyrexia, Renal Failure Acute, Vomiting
on Jul 15, 2010 Female patient from GERMANY , 57 years of age, was diagnosed with diabetes mellitus and was treated with Glucophage (View Usage). Patient experienced the following unwanted or unexpected effects: cardiogenic shock, dehydration, diarrhoea, lactic acidosis, pyrexia, renal failure acute, vomiting. Glucophage dosage: . During the same period patient was treated with REPAGLINIDE (View Repaglinide Review and Repaglinide Label ), MICARDIS HCT (View Micardis Hct Review and Micardis Hct Label ), LASIX (View Lasix Review and Lasix Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), PROPAFENONE HCL (View Propafenone Hcl Review and Propafenone Hcl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), CEFTRIAXONE (View Ceftriaxone Review and Ceftriaxone Label ).

6870941-4 | Accident, Cardio-respiratory Arrest, Heart Injury, Lactic Acidosis, Multi-organ Failure, Renal Failure Acute, Sternal Fracture
Patient was taking Glucophage (View Usage). Patient had the following side effects: accident, cardio-respiratory arrest, heart injury, lactic acidosis, multi-organ failure, renal failure acute, sternal fracture on Jul 15, 2010 from GERMANY Additional patient health information: Male patient , 78 years of age, . Glucophage dosage: Renitec Was Taken As Conmed.. During the same period patient was treated with ENALAPRIL MALEATE (View Enalapril Maleate Review and Enalapril Maleate Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), GLUCOR (View Glucor Review and Glucor Label ), PRAXILENE (View Praxilene Review and Praxilene Label ). Patient was hospitalized.

6862298-X | Cytolytic Hepatitis
Adverse event was reported on Jul 12, 2010 by a Female patient taking Glucophage (View Usage) (Dosage: ) was diagnosed with type 2 diabetes mellitus, urticaria and. Location: GERMANY , 50 years of age, After Glucophage was administered, patient had the following side effects: cytolytic hepatitis. During the same period patient was treated with TINSET (View Tinset Review and Tinset Label ), POLARAMINE (View Polaramine Review and Polaramine Label ). Patient was hospitalized.

6862274-7 | International Normalised Ratio Increased, Lactic Acidosis
on Jul 11, 2010 Female patient from GERMANY , 65 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Glucophage (View Usage). Patient experienced the following unwanted or unexpected effects: international normalised ratio increased, lactic acidosis. Glucophage dosage: Glucophage At A Dose Of 500mg. During the same period patient was treated with RAMIPRIL (View Ramipril Review and Ramipril Label ), BISOPROLOL FUMARATE (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), INSULIN (View Insulin Review and Insulin Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ). Patient was hospitalized.

6860876-5 | Hyperkalaemia, Nausea, Renal Failure Acute
on Jul 09, 2010 Male patient from GERMANY , 63 years of age, was diagnosed with type 2 diabetes mellitus, essential hypertension and was treated with Glucophage (View Usage). Patient had the following side effects: hyperkalaemia, nausea (What is nausea?), renal failure acute. Glucophage dosage: 1 Df = Gm3. During the same period patient was treated with ENALAPRIL MALEATE (1df=20mgd) (View Enalapril Maleate Review and Enalapril Maleate Label ), VICTOZA (View Victoza Review and Victoza Label ), LIPITOR (View Lipitor Review and Lipitor Label ), ZOLPIDEM (View Zolpidem Review and Zolpidem Label ), DUROFERON (View Duroferon Review and Duroferon Label ), TROMBYL (View Trombyl Review and Trombyl Label ), BEZALIP RETARD (View Bezalip Retard Review and Bezalip Retard Label ), PLAVIX (Film Coated) (View Plavix Review and Plavix Label ). Patient was hospitalized.

6855219-7 | Blood Lactic Acid Increased, Decreased Appetite, Dehydration, Diarrhoea, Hypoglycaemia, Renal Failure Acute, Vomiting
Patient was taking Glucophage (View Usage). After Glucophage was administered, patient had the following side effects: blood lactic acid increased, decreased appetite, dehydration, diarrhoea, hypoglycaemia, renal failure acute, vomiting on Jul 08, 2010 from GERMANY Additional patient health information: Female patient , 84 years of age, was diagnosed with gout (What is gout?) and. Glucophage dosage: . During the same period patient was treated with COKENZEN (View Cokenzen Review and Cokenzen Label ), INIPOMP (View Inipomp Review and Inipomp Label ), DIAMICRON (View Diamicron Review and Diamicron Label ), XELEVIA (View Xelevia Review and Xelevia Label ), COLCHIMAX (View Colchimax Review and Colchimax Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ). Patient was hospitalized.

6839708-7 | Hypoglycaemia, Hypothermia
Adverse event was reported on Jul 02, 2010 by a Male patient taking Glucophage (View Usage) (Dosage: ) . Location: GERMANY , 77 years of age, Patient experienced the following unwanted or unexpected effects: hypoglycaemia, hypothermia (What is hypothermia?). During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), LANTUS (30ui Until Mar09 And It Was Reduced To 12 Iu) (View Lantus Review and Lantus Label ). Patient was hospitalized.

6839028-0 | Dermatitis Bullous
on Jul 02, 2010 Male patient from GERMANY , 54 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Glucophage (View Usage). Patient had the following side effects: dermatitis bullous. Glucophage dosage: . During the same period patient was treated with EXFORGE (View Exforge Review and Exforge Label ). Patient was hospitalized.

6839027-9 | Angioedema, Dysphagia, Dysphonia
on Jul 02, 2010 Male patient from GERMANY , 67 years of age, was diagnosed with type 2 diabetes mellitus, hypertension and was treated with Glucophage (View Usage). After Glucophage was administered, patient had the following side effects: angioedema, dysphagia, dysphonia. Glucophage dosage: Coated Tab Interrupted On 19jun2010(4d) Restarted On Unk Date. During the same period patient was treated with TRIATEC (10 Mg Tabs) (View Triatec Review and Triatec Label ). Patient was hospitalized.

6839026-7 | Hyperlactacidaemia, Hypotension, Myocardial Ischaemia, Renal Impairment
Patient was taking Glucophage (View Usage). Patient experienced the following unwanted or unexpected effects: hyperlactacidaemia, hypotension, myocardial ischaemia, renal impairment on Jul 02, 2010 from GERMANY Additional patient health information: Male patient , 84 years of age, was diagnosed with type 2 diabetes mellitus and. Glucophage dosage: 850 Mg. During the same period patient was treated with AMIODARONE HCL (View Amiodarone Hcl Review and Amiodarone Hcl Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), LASIX (View Lasix Review and Lasix Label ), PREVISCAN (View Previscan Review and Previscan Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), DIFFU K (View Diffu-k Review and Diffu-k Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

6827156-5 | Abdominal Pain Lower, Decreased Appetite, Gait Disturbance, Hearing Impaired, Muscle Atrophy, Oedema Peripheral, Scab, Weight Decreased
Adverse event was reported on Jun 29, 2010 by a Female patient taking Glucophage (View Usage) (Dosage: ) . Location: GERMANY , 70 years of age, Patient had the following side effects: abdominal pain lower, decreased appetite, gait disturbance, hearing impaired, muscle atrophy, oedema peripheral, scab (What is scab?), weight decreased.

6826337-4 | Anaemia, Diarrhoea, Hyperkalaemia, Lactic Acidosis, Renal Failure Acute, Vomiting, White Blood Cell Count Increased
on Jun 28, 2010 Female patient from GERMANY , 84 years of age, was diagnosed with type 2 diabetes mellitus, hypertension and was treated with Glucophage (View Usage). After Glucophage was administered, patient had the following side effects: anaemia, diarrhoea, hyperkalaemia, lactic acidosis, renal failure acute, vomiting, white blood cell count increased. Glucophage dosage: . During the same period patient was treated with TRIATEC (View Triatec Review and Triatec Label ), LASIX (View Lasix Review and Lasix Label ), ASPEGIC 1000 (View Aspegic 1000 Review and Aspegic 1000 Label ), PLAVIX (View Plavix Review and Plavix Label ), CARDENSIEL (View Cardensiel Review and Cardensiel Label ). Patient was hospitalized.

6820545-4 | Abdominal Pain, Bronchitis, Dehydration, Lactic Acidosis, Nausea, Renal Failure Acute
on Jun 28, 2010 Female patient from GERMANY , 50 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Glucophage (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), bronchitis (What is bronchitis?), dehydration, lactic acidosis, nausea (What is nausea?), renal failure acute. Glucophage dosage: . During the same period patient was treated with BI PROFENID (150mg) (View Bi-profenid Review and Bi-profenid Label ), JANUVIA (Tabs. At Night) (View Januvia Review and Januvia Label ). Patient was hospitalized.

6809489-1 | Cataract
Patient was taking Glucophage (View Usage). Patient had the following side effects: cataract (What is cataract?) on Jun 18, 2010 from CHINA Additional patient health information: Male patient , 75 years of age, was diagnosed with diabetes mellitus and. Glucophage dosage: .

6809300-9 | Hypoglycaemia, Somnolence
Adverse event was reported on Jun 21, 2010 by a Male patient taking Glucophage (View Usage) (Dosage: ) . Location: GERMANY , 76 years of age, After Glucophage was administered, patient had the following side effects: hypoglycaemia, somnolence. During the same period patient was treated with LANTUS (Discontinued On 27mar10 Re-introduced On An Unk Date) (View Lantus Review and Lantus Label ), ACTOS (View Actos Review and Actos Label ), AMARYL (View Amaryl Review and Amaryl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), MEVALOTIN (View Mevalotin Review and Mevalotin Label ), DETRUSITOL (View Detrusitol Review and Detrusitol Label ). Patient was hospitalized.

6803639-9 | Chest Pain, Dehydration, Diarrhoea, Grand Mal Convulsion, Haemodialysis, Renal Failure Acute, Renal Tubular Necrosis, Vomiting
on Jun 17, 2010 Female patient from GERMANY , 52 years of age, was treated with Glucophage (View Usage). Patient experienced the following unwanted or unexpected effects: chest pain (What is chest pain?), dehydration, diarrhoea, grand mal convulsion, haemodialysis, renal failure acute, renal tubular necrosis, vomiting. Glucophage dosage: . During the same period patient was treated with IOMERON 150 (View Iomeron-150 Review and Iomeron-150 Label ), OMNIPAQUE 140 (View Omnipaque 140 Review and Omnipaque 140 Label ), LORAZEPAM (2.5 Mg Tabs) (View Lorazepam Review and Lorazepam Label ), DIAMICRON (View Diamicron Review and Diamicron Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), RISPERDAL (View Risperdal Review and Risperdal Label ), ZOLPIDEM (Tablet) (View Zolpidem Review and Zolpidem Label ). Patient was hospitalized.

6794814-0 | Hypoglycaemia, Somnolence
on Jun 17, 2010 Male patient from GERMANY , 76 years of age, was treated with Glucophage (View Usage). Patient had the following side effects: hypoglycaemia, somnolence. Glucophage dosage: . During the same period patient was treated with LANTUS (Discontinued On 27mar10 Re-introduced On An Unk Date) (View Lantus Review and Lantus Label ), ACTOS (View Actos Review and Actos Label ), AMARYL (View Amaryl Review and Amaryl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), MEVALOTIN (View Mevalotin Review and Mevalotin Label ), DETRUSITOL (View Detrusitol Review and Detrusitol Label ). Patient was hospitalized.

6794771-7 | Coma, Fall, Herpes Zoster, Pneumonia Aspiration, Renal Failure Acute, Respiratory Distress, Sciatica, Shock
Patient was taking Glucophage (View Usage). After Glucophage was administered, patient had the following side effects: coma, fall (What is fall?), herpes zoster, pneumonia aspiration, renal failure acute, respiratory distress, sciatica (What is sciatica?), shock on Jun 17, 2010 from GERMANY Additional patient health information: Female patient , 73 years of age, was diagnosed with type 2 diabetes mellitus, hypertension, sciatica (What is sciatica?), herpes zoster, neuralgia, osteoporosis (What is osteoporosis?) and. Glucophage dosage: . During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), TOPALGIC (200mg:21apr2010-27apr2010:6(d) 400mg:28apr2010-29apr2010:1(d)) (View Topalgic Review and Topalgic Label ), ZELITREX (View Zelitrex Review and Zelitrex Label ), GABAPENTINE (View Gabapentine Review and Gabapentine Label ), LASIX (40mg Tabs) (View Lasix Review and Lasix Label ), TENSTATEN (50 Mg Caps) (View Tenstaten Review and Tenstaten Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), ACTONEL (35 Mg Tabs; 0.1429 Df) (View Actonel Review and Actonel Label ). Patient was hospitalized.

6772823-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Back Pain, Cytolytic Hepatitis
Adverse event was reported on Jun 09, 2010 by a Male patient taking Glucophage (View Usage) (Dosage: ) was diagnosed with diabetes mellitus, back pain (What is back pain?), depression (What is depression?), hypertension, dyslipidaemia, atrial fibrillation (What is atrial fibrillation?), essential tremor and. Location: FRANCE , 73 years of age, Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, back pain (What is back pain?), cytolytic hepatitis. During the same period patient was treated with DAFALGAN (View Dafalgan Review and Dafalgan Label ), CITALOPRAM HYDROBROMIDE (View Citalopram Hydrobromide Review and Citalopram Hydrobromide Label ), PERINDOPRIL (View Perindopril Review and Perindopril Label ), THIOCOLCHICOSIDE (View Thiocolchicoside Review and Thiocolchicoside Label ), LIPANTHYL (View Lipanthyl Review and Lipanthyl Label ), PREVISCAN (Previscan 20 Mg Tabs) (View Previscan Review and Previscan Label ), TOPALGIC LP (View Topalgic Lp Review and Topalgic Lp Label ), MYSOLINE (Mysoline 250mg Tabs) (View Mysoline Review and Mysoline Label ). Patient was hospitalized.

6770895-5 | Cardiogenic Shock, Dehydration, Diarrhoea, Erythema, Haemodialysis, Hypotension, Lactic Acidosis, Pain
on Jun 04, 2010 Female patient from GERMANY , 57 years of age, was diagnosed with diabetes mellitus and was treated with Glucophage (View Usage). Patient had the following side effects: cardiogenic shock, dehydration, diarrhoea, erythema, haemodialysis, hypotension, lactic acidosis, pain (What is pain?). Glucophage dosage: . During the same period patient was treated with REPAGLINIDE (View Repaglinide Review and Repaglinide Label ), MICARDIS HCT (View Micardis Hct Review and Micardis Hct Label ), LASIX (View Lasix Review and Lasix Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), PROPAFENONE HCL (View Propafenone Hcl Review and Propafenone Hcl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), CEFTRIAXONE (View Ceftriaxone Review and Ceftriaxone Label ).

6768914-5 | Caesarean Section, Normal Newborn, Phlebitis, Pregnancy
on Jun 03, 2010 Female patient from GERMANY , 34 years of age, was diagnosed with diabetes mellitus and was treated with Glucophage (View Usage). After Glucophage was administered, patient had the following side effects: caesarean section, normal newborn, phlebitis, pregnancy (What is pregnancy?). Glucophage dosage: . During the same period patient was treated with INSULIN (View Insulin Review and Insulin Label ). Patient was hospitalized.

6767553-X | Cardiogenic Shock, Dehydration, Diarrhoea, Lactic Acidosis, Renal Failure Acute, Vomiting
Patient was taking Glucophage (View Usage). Patient experienced the following unwanted or unexpected effects: cardiogenic shock, dehydration, diarrhoea, lactic acidosis, renal failure acute, vomiting on May 24, 2010 from GERMANY Additional patient health information: Female patient , 57 years of age, was diagnosed with diabetes mellitus and. Glucophage dosage: . During the same period patient was treated with REPAGLINIDE (View Repaglinide Review and Repaglinide Label ), MICARDIS HCT (View Micardis Hct Review and Micardis Hct Label ), LASIX (View Lasix Review and Lasix Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), PROPAFENONE HCL (View Propafenone Hcl Review and Propafenone Hcl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

6767052-5 | Diarrhoea, Hypoglycaemia, Lactic Acidosis, Renal Failure, Tachypnoea, Vomiting
Adverse event was reported on May 24, 2010 by a Male patient taking Glucophage (View Usage) (Dosage: ) was diagnosed with type 2 diabetes mellitus and. Location: GERMANY , 74 years of age, Patient had the following side effects: diarrhoea, hypoglycaemia, lactic acidosis, renal failure, tachypnoea, vomiting. During the same period patient was treated with REPAGLINIDE (1df=3u.1000mg) (View Repaglinide Review and Repaglinide Label ), TAMSULOSIN HCL (View Tamsulosin Hcl Review and Tamsulosin Hcl Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), OLPRESS (View Olpress Review and Olpress Label ), LOBIVON (View Lobivon Review and Lobivon Label ), LASIX (View Lasix Review and Lasix Label ). Patient was hospitalized.

6767051-3 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Back Pain, Cytolytic Hepatitis
on May 28, 2010 Male patient from FRANCE , 73 years of age, was diagnosed with diabetes mellitus, back pain (What is back pain?), depression (What is depression?), hypertension, atrial fibrillation (What is atrial fibrillation?), essential tremor and was treated with Glucophage (View Usage). After Glucophage was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, back pain (What is back pain?), cytolytic hepatitis. Glucophage dosage: . During the same period patient was treated with DAFALGAN (View Dafalgan Review and Dafalgan Label ), CITALOPRAM (View Citalopram Review and Citalopram Label ), PERINDOPRIL (View Perindopril Review and Perindopril Label ), THIOCOLCHICOSIDE (View Thiocolchicoside Review and Thiocolchicoside Label ), LIPANTHYL (View Lipanthyl Review and Lipanthyl Label ), PREVISCAN (View Previscan Review and Previscan Label ), TOPALGIC LP (View Topalgic Lp Review and Topalgic Lp Label ), MYSOLINE (View Mysoline Review and Mysoline Label ). Patient was hospitalized.

6767049-5 | Hyperkalaemia, Metabolic Acidosis, Renal Failure Acute
on May 19, 2010 Female patient from GERMANY , 77 years of age, was diagnosed with type 2 diabetes mellitus and was treated with Glucophage (View Usage). Patient experienced the following unwanted or unexpected effects: hyperkalaemia, metabolic acidosis, renal failure acute. Glucophage dosage: . During the same period patient was treated with BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), MICARDIS (View Micardis Review and Micardis Label ), LASIX (View Lasix Review and Lasix Label ), FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ). Patient was hospitalized.

6765967-5 | International Normalised Ratio Increased, Lactic Acidosis
Patient was taking Glucophage (View Usage). Patient had the following side effects: international normalised ratio increased, lactic acidosis on May 19, 2010 from ITALY Additional patient health information: Female patient , 65 years of age, was diagnosed with type 2 diabetes mellitus and. Glucophage dosage: Glucophage At A Dose Of 500mg. During the same period patient was treated with RAMIPRIL (View Ramipril Review and Ramipril Label ), BISOPROLOL FUMARATE (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), INSULIN (View Insulin Review and Insulin Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ). Patient was hospitalized.

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Glucophage Questions, Answers, Feedback and Comments

Comments to date: 1. Page 1 of 1.

isra   amman

2:56pm on Monday, August 31st, 2009

Glucophage causing to me severe hypotension - can reach 8050 .. and diarrhea with abdominal cramps .... read more »

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 Glucophage 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 Glucophage quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Glucophage 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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Glucophage Reactions
Abdominal Discomfort
Abdominal PainWhat is Abdominal pain?
Anaemia
Anorexia
Asthenia
Blood Glucose Decreased
Blood Glucose Increased
Cerebrovascular Accident
Death
Dehydration
Diarrhoea
DizzinessWhat is Dizziness?
Dyspnoea
FallWhat is Fall?
Fatigue
HeadacheWhat is Headache?
Hyperkalaemia
Hypoglycaemia
Lactic Acidosis
Metabolic Acidosis
Multi-organ Failure
Myocardial Infarction
NauseaWhat is Nausea?
Overdose
PregnancyWhat is Pregnancy?
Renal Failure
Renal Failure Acute
Shock
Vomiting
Weight Decreased
Glucophage 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 Glucophage 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!