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Summary

FDA Adverse Reports: 137. View All

Fortum FDA safety alerts: No

Reported deaths: 22

Reported hospitalizations: 97

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

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Showing 1-50 of 137  Next Page  >

6862907-5 | Cardio-respiratory Arrest, Crying, Cyanosis, Hypotonia, Pallor, Syncope
on Jul 15, 2010 Female patient from FRANCE , weighting 5.95 lb, was treated with Fortum (View Usage). Patient experienced the following unwanted or unexpected effects: cardio-respiratory arrest, crying, cyanosis, hypotonia, pallor, syncope. Fortum dosage: 90mg Single Dose.

6862902-6 | Dermatitis Exfoliative
Patient was taking Fortum (View Usage). Patient had the following side effects: dermatitis exfoliative on Jul 13, 2010 from CHINA Additional patient health information: Male patient , 63 years of age, was diagnosed with infection (What is infection?) and. Fortum dosage: .2g Per Day.

6814698-1 | Leukopenia, Neutropenia
Adverse event was reported on Jul 01, 2010 by a Male patient taking Fortum (View Usage) (Dosage: ) was diagnosed with pain (What is pain?) and. Location: FRANCE , weighting 37.48 lb, After Fortum was administered, patient had the following side effects: leukopenia, neutropenia. During the same period patient was treated with FLAGYL (107mg Three Times Per Day) (View Flagyl Review and Flagyl Label ), VANCOMYCIN HCL (View Vancomycin Hcl Review and Vancomycin Hcl Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ), CLAFORAN (280mg Three Times Per Day) (View Claforan Review and Claforan Label ), TRIFLUCAN (View Triflucan Review and Triflucan Label ), NALBUPHINE (View Nalbuphine Review and Nalbuphine Label ), PERFALGAN (View Perfalgan Review and Perfalgan Label ), NEXIUM (View Nexium Review and Nexium Label ). Patient was hospitalized.

6803227-4 | Dermatitis Exfoliative
on Jun 17, 2010 Male patient from CHINA , 63 years of age, was diagnosed with infection (What is infection?) and was treated with Fortum (View Usage). Patient experienced the following unwanted or unexpected effects: dermatitis exfoliative. Fortum dosage: .2g Per Day.


6758543-1 | Anaphylactoid Reaction, Blood Pressure Decreased, Chest Discomfort, Hyperaemia, Hyperhidrosis
on May 28, 2010 Female patient from RUSSIAN FEDERATION , 55 years of age, was diagnosed with thrombosis prophylaxis, detoxification and was treated with Fortum (View Usage). Patient had the following side effects: anaphylactoid reaction, blood pressure decreased, chest discomfort, hyperaemia, hyperhidrosis. Fortum dosage: 6g Per Day. During the same period patient was treated with ENOXAPARIN SODIUM (View Enoxaparin Sodium Review and Enoxaparin Sodium Label ), DEXTROSE (View Dextrose Review and Dextrose Label ), SODIUM CHLORIDE (View Sodium Chloride Review and Sodium Chloride Label ).

6749679-X | Convulsion
Patient was taking Fortum (View Usage). After Fortum was administered, patient had the following side effects: convulsion on May 24, 2010 from MALAYSIA Additional patient health information: Male patient , 52 years of age, . Fortum dosage: . During the same period patient was treated with CLOXACILLIN (View Cloxacillin Review and Cloxacillin Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), VITAMIN B COMPLEX CAP (View Vitamin B Complex Cap Review and Vitamin B Complex Cap Label ), CALCIUM CARBONATE (View Calcium Carbonate Review and Calcium Carbonate Label ), ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid Label ).

6685088-X | Agranulocytosis, Granulocytes Maturation Arrest, Neutropenia, Pancytopenia
Adverse event was reported on Apr 12, 2010 by a Male patient taking Fortum (View Usage) (Dosage: 1g Per Day) . Location: FRANCE , 74 years of age, Patient experienced the following unwanted or unexpected effects: agranulocytosis, granulocytes maturation arrest, neutropenia, pancytopenia. During the same period patient was treated with PYOSTACINE (4unit Per Day) (View Pyostacine Review and Pyostacine Label ), MIRTAZAPINE (15mg Per Day) (View Mirtazapine Review and Mirtazapine Label ), LEVOTHYROX (View Levothyrox Review and Levothyrox Label ), XANAX (View Xanax Review and Xanax Label ), SERESTA (View Seresta Review and Seresta Label ), LASILIX FAIBLE (View Lasilix Faible Review and Lasilix Faible Label ), FORLAX (View Forlax Review and Forlax Label ), ACETYLCYSTEINE (View Acetylcysteine Review and Acetylcysteine Label ). Patient was hospitalized.

6651558-3 | Blood Pressure Increased, Chest Discomfort, Gastritis, Nausea, Product Quality Issue, Rash
on Mar 11, 2010 Male patient from INDIA , 45 years of age, was treated with Fortum (View Usage). Patient had the following side effects: blood pressure increased, chest discomfort, gastritis, nausea (What is nausea?), product quality issue, rash (What is rash?). Fortum dosage: .

6626129-5 | Rash Pruritic
on Mar 04, 2010 Female patient from RUSSIAN FEDERATION , 27 years of age, was treated with Fortum (View Usage). After Fortum was administered, patient had the following side effects: rash pruritic. Fortum dosage: . During the same period patient was treated with MAGNESIUM SULFATE (View Magnesium Sulfate Review and Magnesium Sulfate Label ), FERRUM (View Ferrum Review and Ferrum Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ).

6602404-5 | Blood Pressure Increased, Chest Discomfort, Gastritis, Nausea, Product Quality Issue, Rash
Patient was taking Fortum (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, chest discomfort, gastritis, nausea (What is nausea?), product quality issue, rash (What is rash?) on Feb 18, 2010 from INDIA Additional patient health information: Male patient , 45 years of age, . Fortum dosage: .

6552670-X | Agranulocytosis, Febrile Neutropenia, Lung Disorder
Adverse event was reported on Jan 19, 2010 by a Female patient taking Fortum (View Usage) (Dosage: ) was diagnosed with immunoglobulins decreased and. Location: FRANCE , 55 years of age, Patient had the following side effects: agranulocytosis, febrile neutropenia, lung disorder. During the same period patient was treated with TAVANIC (View Tavanic Review and Tavanic Label ), PROGRAF (View Prograf Review and Prograf Label ), CELLCEPT (View Cellcept Review and Cellcept Label ), VALGANCICLOVIR HCL (View Valganciclovir Hcl Review and Valganciclovir Hcl Label ), SANDOGLOBULIN (72g Per Day) (View Sandoglobulin Review and Sandoglobulin Label ), REHYDRATION (View Rehydration Review and Rehydration Label ). Patient was hospitalized.

6329451-5 | Excoriation, Rash, Toxic Epidermal Necrolysis
on Aug 20, 2009 Male patient from CHINA , 40 years of age, was diagnosed with infection (What is infection?) and was treated with Fortum (View Usage). After Fortum was administered, patient had the following side effects: excoriation, rash (What is rash?), toxic epidermal necrolysis. Fortum dosage: 2g Twice Per Day. Patient was hospitalized.

6294726-5 | Anaphylactic Shock, Cardio-respiratory Arrest, Metabolic Acidosis, Oedema Mucosal, Vomiting
on Jul 24, 2009 Female patient from GERMANY , weighting 26.46 lb, was diagnosed with febrile neutropenia and was treated with Fortum (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock, cardio-respiratory arrest, metabolic acidosis, oedema mucosal, vomiting. Fortum dosage: 450mg Three Times Per Day. During the same period patient was treated with MORONAL (1ml Three Times Per Day) (View Moronal Review and Moronal Label ).

6275346-5 | Anaphylactic Shock, Cardio-respiratory Arrest, Metabolic Acidosis, Oedema Mucosal, Vomiting
Patient was taking Fortum (View Usage). Patient had the following side effects: anaphylactic shock, cardio-respiratory arrest, metabolic acidosis, oedema mucosal, vomiting on Jul 16, 2009 from GERMANY Additional patient health information: Female patient , weighting 26.46 lb, was diagnosed with febrile neutropenia and. Fortum dosage: 450mg Three Times Per Day. During the same period patient was treated with MORONAL (1ml Three Times Per Day) (View Moronal Review and Moronal Label ).

6258726-3 | Erythema, Eye Inflammation, Haemorrhage Intracranial, Stevens-johnson Syndrome
Adverse event was reported on Jul 06, 2009 by a Male patient taking Fortum (View Usage) (Dosage: 2g Twice Per Day) . Location: INDIA , 40 years of age, weighting 90.39 lb, After Fortum was administered, patient had the following side effects: erythema, eye inflammation, haemorrhage intracranial, stevens-johnson syndrome. During the same period patient was treated with AMIKACIN (500mg Twice Per Day) (View Amikacin Review and Amikacin Label ), FLUCONAZOLE (View Fluconazole Review and Fluconazole Label ), MANITOL (View Manitol Review and Manitol Label ), AMINOPHYLLINE (View Aminophylline Review and Aminophylline Label ), NEVIRAPINE (View Nevirapine Review and Nevirapine Label ), LAMIVUDINE (View Lamivudine Review and Lamivudine Label ), STAVUDINE (View Stavudine Review and Stavudine Label ).

6252955-0 | Erythema, Eye Inflammation, Stevens-johnson Syndrome
on Jun 22, 2009 Male patient from INDIA , 40 years of age, weighting 90.39 lb, was treated with Fortum (View Usage). Patient experienced the following unwanted or unexpected effects: erythema, eye inflammation, stevens-johnson syndrome. Fortum dosage: 2mg Twice Per Day. During the same period patient was treated with AMIKACIN (500mg Twice Per Day) (View Amikacin Review and Amikacin Label ), FLUCONAZOLE (View Fluconazole Review and Fluconazole Label ), MANITOL (View Manitol Review and Manitol Label ), AMINOPHYLLINE (View Aminophylline Review and Aminophylline Label ), NEVIRAPINE (View Nevirapine Review and Nevirapine Label ), LAMIVUDINE (View Lamivudine Review and Lamivudine Label ), STAVUDINE (View Stavudine Review and Stavudine Label ).

6192000-9 | Extrapyramidal Disorder, Hyperplasia, Marrow Hyperplasia, Meningitis, Pyrexia
on May 05, 2009 Male patient from FRANCE , 15 years of age, was treated with Fortum (View Usage). Patient had the following side effects: extrapyramidal disorder, hyperplasia, marrow hyperplasia, meningitis (What is meningitis?), pyrexia. Fortum dosage: . During the same period patient was treated with FOSCAVIR (View Foscavir Review and Foscavir Label ), CYMEVAN (View Cymevan Review and Cymevan Label ), TARGOCID (View Targocid Review and Targocid Label ). Patient was hospitalized.

6124633-X | Anxiety, Confusional State, Malaise, Myoclonus, Overdose, Renal Failure Acute, Somnolence
Patient was taking Fortum (View Usage). After Fortum was administered, patient had the following side effects: anxiety (What is anxiety?), confusional state, malaise, myoclonus, overdose, renal failure acute, somnolence on Mar 09, 2009 from FRANCE Additional patient health information: Female patient , 68 years of age, . Fortum dosage: 6g Per Day. During the same period patient was treated with CIFLOX (500mg Twice Per Day) (View Ciflox Review and Ciflox Label ), NEORAL (110mg Per Day) (View Neoral Review and Neoral Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ), CELLCEPT (1g Per Day) (View Cellcept Review and Cellcept Label ), AMLOR (View Amlor Review and Amlor Label ), DETENSIEL (View Detensiel Review and Detensiel Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), INIPOMP (View Inipomp Review and Inipomp Label ). Patient was hospitalized.

6100084-9 | Pruritus, Rash, Thrombocytopenia
Adverse event was reported on Feb 25, 2009 by a Male patient taking Fortum (View Usage) (Dosage: ) was diagnosed with pneumonia (What is pneumonia?) and. Location: MALAYSIA , child 6 years of age, Patient experienced the following unwanted or unexpected effects: pruritus, rash (What is rash?), thrombocytopenia. During the same period patient was treated with CLOXACILLIN (View Cloxacillin Review and Cloxacillin Label ).

6100082-5 | Delirium, Thinking Abnormal
on Feb 25, 2009 Female patient from MALAYSIA , 73 years of age, was diagnosed with infection (What is infection?) and was treated with Fortum (View Usage). Patient had the following side effects: delirium, thinking abnormal. Fortum dosage: . During the same period patient was treated with RANITIDINE (View Ranitidine Review and Ranitidine Label ), DIGOXIN (View Digoxin Review and Digoxin Label ).

6100081-3 | Confusional State, Delirium, Disorientation, Dyskinesia
on Feb 25, 2009 Female patient from MALAYSIA , 60 years of age, was diagnosed with infection (What is infection?) and was treated with Fortum (View Usage). After Fortum was administered, patient had the following side effects: confusional state, delirium, disorientation, dyskinesia. Fortum dosage: . During the same period patient was treated with TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ), METOPROLOL (View Metoprolol Review and Metoprolol Label ).

6100040-0 | Erythema, Hypersensitivity, Rash, Rash Maculo-papular
Patient was taking Fortum (View Usage). Patient experienced the following unwanted or unexpected effects: erythema, hypersensitivity, rash (What is rash?), rash maculo-papular on Feb 20, 2009 from FRANCE Additional patient health information: Male patient , 71 years of age, was diagnosed with colostomy infection and. Fortum dosage: 3g Per Day. During the same period patient was treated with VANCOMYCIN HCL (View Vancomycin Hcl Review and Vancomycin Hcl Label ), AMIKLIN (View Amiklin Review and Amiklin Label ), TIENAM (View Tienam Review and Tienam Label ), CIFLOX (View Ciflox Review and Ciflox Label ), PIPERACILLIN (View Piperacillin Review and Piperacillin Label ). Patient was hospitalized.

6087359-7 | Cholestasis
Adverse event was reported on Feb 12, 2009 by a Male patient taking Fortum (View Usage) (Dosage: 1g Three Times Per Day) was diagnosed with lung infection, pain (What is pain?) and. Location: FRANCE , 75 years of age, Patient had the following side effects: cholestasis. During the same period patient was treated with TAZOCILLINE (4g Three Times Per Day) (View Tazocilline Review and Tazocilline Label ), FLAGYL (500mg Three Times Per Day) (View Flagyl Review and Flagyl Label ), CANCIDAS (50mg Per Day) (View Cancidas Review and Cancidas Label ), NEUPOGEN (View Neupogen Review and Neupogen Label ), NEXIUM (40mg Per Day) (View Nexium Review and Nexium Label ), PERFALGAN (View Perfalgan Review and Perfalgan Label ), CALCIUM GLUCONATE (View Calcium Gluconate Review and Calcium Gluconate Label ), OFLOCET (200mg Twice Per Day) (View Oflocet Review and Oflocet Label ).

6061663-0 | Antibiotic Level Above Therapeutic, Convulsion
on Jan 23, 2009 Male patient from FRANCE , 69 years of age, was treated with Fortum (View Usage). After Fortum was administered, patient had the following side effects: antibiotic level above therapeutic, convulsion. Fortum dosage: 4g Per Day. During the same period patient was treated with MECHANICAL VENTILATION (View Mechanical Ventilation Review and Mechanical Ventilation Label ). Patient was hospitalized.

6061661-7 | Aspergillosis, Pruritus
on Jan 21, 2009 Male patient from FRANCE , 46 years of age, was diagnosed with aspergillosis and was treated with Fortum (View Usage). Patient experienced the following unwanted or unexpected effects: aspergillosis, pruritus. Fortum dosage: . During the same period patient was treated with ZOVIRAX (View Zovirax Review and Zovirax Label ), TRUVADA (1unit Per Day) (View Truvada Review and Truvada Label ), RALTEGRAVIR (1unit Twice Per Day) (View Raltegravir Review and Raltegravir Label ), PREZISTA (2unit Twice Per Day) (View Prezista Review and Prezista Label ), NORVIR (1unit Twice Per Day) (View Norvir Review and Norvir Label ), PENTACARINAT (View Pentacarinat Review and Pentacarinat Label ), VFEND (View Vfend Review and Vfend Label ), WELLVONE (View Wellvone Review and Wellvone Label ). Patient was hospitalized.

6056894-X | Agitation, Body Temperature Increased, Chills, Cholestasis, Confusional State, Disorientation, Hallucination, Auditory
Patient was taking Fortum (View Usage). Patient had the following side effects: agitation, body temperature increased, chills, cholestasis, confusional state, disorientation, hallucination, auditory on Jan 19, 2009 from FRANCE Additional patient health information: Male patient , 46 years of age, . Fortum dosage: . During the same period patient was treated with VFEND (View Vfend Review and Vfend Label ), PROGRAF (View Prograf Review and Prograf Label ), CELLCEPT (View Cellcept Review and Cellcept Label ), NEXIUM (20mg Per Day) (View Nexium Review and Nexium Label ), LANSOPRAZOLE (15mg Per Day) (View Lansoprazole Review and Lansoprazole Label ), ZYVOXID (View Zyvoxid Review and Zyvoxid Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ). Patient was hospitalized.

6056890-2 | Beta 2 Microglobulin Increased, C-reactive Protein Increased, Eosinophilia, Erythema, Face Oedema, Gamma-glutamyltransferase Increased, Lymphadenopathy, Normochromic Normocytic Anaemia
Adverse event was reported on Jan 19, 2009 by a Male patient taking Fortum (View Usage) (Dosage: 1unit Four Times Per Day) was diagnosed with osteoarthritis (What is osteoarthritis?) and. Location: FRANCE , 79 years of age, After Fortum was administered, patient had the following side effects: beta 2 microglobulin increased, c-reactive protein increased, eosinophilia, erythema, face oedema, gamma-glutamyltransferase increased, lymphadenopathy, normochromic normocytic anaemia. During the same period patient was treated with CIFLOX (View Ciflox Review and Ciflox Label ), NITRODERM (View Nitroderm Review and Nitroderm Label ), ADANCOR (View Adancor Review and Adancor Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), LASILIX (View Lasilix Review and Lasilix Label ), KENZEN (View Kenzen Review and Kenzen Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), ZOXAN (View Zoxan Review and Zoxan Label ). Patient was hospitalized.

6056887-2 | Confusional State, Overdose, Tremor, Weight Decreased
on Jan 19, 2009 Male patient from FRANCE , 75 years of age, weighting 123.5 lb, was treated with Fortum (View Usage). Patient experienced the following unwanted or unexpected effects: confusional state, overdose, tremor, weight decreased. Fortum dosage: 2g Twice Per Day. During the same period patient was treated with CIFLOX (500mg Twice Per Day) (View Ciflox Review and Ciflox Label ). Patient was hospitalized.

6055543-4 | Blood Creatinine Increased, Hyperbilirubinaemia, Hypernatraemia, Interstitial Lung Disease, Murphy's Sign Positive, Neurological Decompensation, Respiratory Distress, Venoocclusive Disease
on Jan 19, 2009 Male patient from FRANCE , 58 years of age, was diagnosed with febrile neutropenia, bone marrow transplant (What is bone marrow transplant?), thrombocytopenia and was treated with Fortum (View Usage). Patient had the following side effects: blood creatinine increased, hyperbilirubinaemia, hypernatraemia, interstitial lung disease, murphy's sign positive, neurological decompensation, respiratory distress, venoocclusive disease. Fortum dosage: . During the same period patient was treated with VANCOMYCIN (View Vancomycin Review and Vancomycin Label ), FLAGYL (View Flagyl Review and Flagyl Label ), BUSULPHAN (View Busulphan Review and Busulphan Label ), FLUDARA (View Fludara Review and Fludara Label ), TAZOCILLINE (View Tazocilline Review and Tazocilline Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ), HYDREA (View Hydrea Review and Hydrea Label ), EXJADE (View Exjade Review and Exjade Label ). Patient was hospitalized.

5987020-0 | International Normalised Ratio Increased
Patient was taking Fortum (View Usage). After Fortum was administered, patient had the following side effects: international normalised ratio increased on Nov 26, 2008 from FRANCE Additional patient health information: Male patient , 82 years of age, was diagnosed with diabetic foot infection, atrial fibrillation (What is atrial fibrillation?) and. Fortum dosage: . During the same period patient was treated with PREVISCAN (View Previscan Review and Previscan Label ), TAZOCILLINE (View Tazocilline Review and Tazocilline Label ), CIPROFLOXACIN HCL (View Ciprofloxacin Hcl Review and Ciprofloxacin Hcl Label ). Patient was hospitalized.

5821457-5 | Agitation, Circulatory Collapse, Haemodynamic Instability, Hypoglycaemia, Hypomagnesaemia, Hypotension, Pigmentation Disorder, Pseudomonas Infection, Septic Shock
Adverse event was reported on Jul 21, 2008 by a Male patient taking Fortum (View Usage) (Dosage: 6g Per Day) was diagnosed with sepsis (What is sepsis?) and. Location: FRANCE , 68 years of age, Patient experienced the following unwanted or unexpected effects: agitation, circulatory collapse, haemodynamic instability, hypoglycaemia, hypomagnesaemia, hypotension, pigmentation disorder, pseudomonas infection, septic shock. During the same period patient was treated with VFEND (View Vfend Review and Vfend Label ), COLIMYCINE (10mu Three Times Per Day) (View Colimycine Review and Colimycine Label ), PAROXETINE HCL (View Paroxetine Hcl Review and Paroxetine Hcl Label ), PREVISCAN (20mg Per Day) (View Previscan Review and Previscan Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), TENORMIN (25mg Three Times Per Day) (View Tenormin Review and Tenormin Label ), TAREG (40mg Per Day) (View Tareg Review and Tareg Label ), ALDACTONE (25mg Per Day) (View Aldactone Review and Aldactone Label ). Patient was hospitalized.

5808822-7 | Asterixis, Cardiac Failure, Catheter Site Haemorrhage, Chromaturia, Confusional State, Ecchymosis, Fatigue, Gastrointestinal Haemorrhage, Haemorrhagic Disorder
on Jul 04, 2008 Male patient from FRANCE , 88 years of age, was treated with Fortum (View Usage). Patient had the following side effects: asterixis, cardiac failure, catheter site haemorrhage, chromaturia, confusional state, ecchymosis, fatigue, gastrointestinal haemorrhage, haemorrhagic disorder. Fortum dosage: 4g Per Day. During the same period patient was treated with CIFLOX (400mg Per Day) (View Ciflox Review and Ciflox Label ), DIAMICRON (1tab Per Day) (View Diamicron Review and Diamicron Label ), DISCOTRINE (10mg Per Day) (View Discotrine Review and Discotrine Label ), INIPOMP (View Inipomp Review and Inipomp Label ), LASIX (1tab Per Day) (View Lasix Review and Lasix Label ), AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), ORBENINE (View Orbenine Review and Orbenine Label ), OFLOCET (View Oflocet Review and Oflocet Label ).

5805987-8 | Rash Maculo-papular, Rash Papular, Rash Pruritic, Skin Exfoliation
on Jun 26, 2007 Male patient from FRANCE , 85 years of age, was treated with Fortum (View Usage). After Fortum was administered, patient had the following side effects: rash maculo-papular, rash papular, rash pruritic, skin exfoliation. Fortum dosage: 2g Twice Per Day. During the same period patient was treated with BACTRIM (3tabs Per Day) (View Bactrim Review and Bactrim Label ), CIFLOX (500mg Three Times Per Day) (View Ciflox Review and Ciflox Label ), PAROXETINE HCL (View Paroxetine Hcl Review and Paroxetine Hcl Label ), LASIX (View Lasix Review and Lasix Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), LEXOMIL (View Lexomil Review and Lexomil Label ), OXYGEN (View Oxygen Review and Oxygen Label ). Patient was hospitalized.

5787942-X | Bloody Discharge, Post Procedural Haemorrhage, Thrombocytopenia
Patient was taking Fortum (View Usage). Patient experienced the following unwanted or unexpected effects: bloody discharge, post procedural haemorrhage, thrombocytopenia on Jun 16, 2008 from FRANCE Additional patient health information: Male patient , 64 years of age, was diagnosed with thrombosis prophylaxis and. Fortum dosage: 6g Per Day. During the same period patient was treated with GENTAMICIN (3mgk Per Day) (View Gentamicin Review and Gentamicin Label ), LOVENOX (4000iu Per Day) (View Lovenox Review and Lovenox Label ), LASILIX FAIBLE 20 MG (40mg Per Day) (View Lasilix Faible 20 Mg Review and Lasilix Faible 20 Mg Label ), INSULATARD (View Insulatard Review and Insulatard Label ), MIXTARD HUMAN 70/30 (View Mixtard Human 70/30 Review and Mixtard Human 70/30 Label ), LANTUS (View Lantus Review and Lantus Label ), PERFALGAN (View Perfalgan Review and Perfalgan Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

5776935-4 | Amnesia, Confusional State, Csf Protein Increased, Disorientation, Incoherent, Meningitis Aseptic, Meningitis Bacterial, Speech Disorder
Adverse event was reported on Jun 09, 2008 by a Female patient taking Fortum (View Usage) (Dosage: 1inj Three Times Per Day) . Location: FRANCE , 85 years of age, Patient had the following side effects: amnesia, confusional state, csf protein increased, disorientation, incoherent, meningitis aseptic, meningitis bacterial, speech disorder. During the same period patient was treated with SOTALEX 80 (View Sotalex 80 Review and Sotalex 80 Label ), LERCAN (View Lercan Review and Lercan Label ), ADANCOR (View Adancor Review and Adancor Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), DESLORATADINE (View Desloratadine Review and Desloratadine Label ), MOPRAL 20 MG (View Mopral 20 Mg Review and Mopral 20 Mg Label ), BACTRIM (View Bactrim Review and Bactrim Label ), TOPALGIC (FRANCE) (View Topalgic (france) Review and Topalgic (france) Label ). Patient was hospitalized.

5758597-5 | Anuria, Pruritus, Rash, Rash Maculo-papular, Renal Failure Acute, Scratch, Skin Lesion
on May 26, 2008 Male patient from FRANCE , 68 years of age, was treated with Fortum (View Usage). After Fortum was administered, patient had the following side effects: anuria, pruritus, rash (What is rash?), rash maculo-papular, renal failure acute, scratch, skin lesion. Fortum dosage: . During the same period patient was treated with ZAVEDOS (12mg Per Day) (View Zavedos Review and Zavedos Label ), ARACYTINE (166mg Per Day) (View Aracytine Review and Aracytine Label ), BELUSTINE (320mg Per Day) (View Belustine Review and Belustine Label ), OFLOCET (View Oflocet Review and Oflocet Label ), VANCOMYCIN HCL (View Vancomycin Hcl Review and Vancomycin Hcl Label ), AMBISOME (View Ambisome Review and Ambisome Label ). Patient was hospitalized.

5752413-3 | Renal Failure
on May 20, 2008 Female patient from FRANCE , 68 years of age, was treated with Fortum (View Usage). Patient experienced the following unwanted or unexpected effects: renal failure. Fortum dosage: 1g Three Times Per Day. During the same period patient was treated with GENTAMICIN (80mg Twice Per Day) (View Gentamicin Review and Gentamicin Label ), ZELITREX (500mg Twice Per Day) (View Zelitrex Review and Zelitrex Label ), VENTOLIN (5mg Three Times Per Day) (View Ventolin Review and Ventolin Label ), LASILIX (40mg Per Day) (View Lasilix Review and Lasilix Label ), PREDNISONE (20mg Per Day) (View Prednisone Review and Prednisone Label ), DOLIPRANE (1000mg Three Times Per Day) (View Doliprane Review and Doliprane Label ), CALCIPARINE (7500iu Twice Per Day) (View Calciparine Review and Calciparine Label ), SOLU MEDROL (20mg Twice Per Day) (View Solu-medrol Review and Solu-medrol Label ). Patient was hospitalized.

5731852-0 | Pruritus, Rash Maculo-papular, Toxic Skin Eruption
Patient was taking Fortum (View Usage). Patient had the following side effects: pruritus, rash maculo-papular, toxic skin eruption on May 06, 2008 from FRANCE Additional patient health information: Female patient , 74 years of age, . Fortum dosage: 1g Per Day. During the same period patient was treated with TIBERAL (4g Per Day) (View Tiberal Review and Tiberal Label ). Patient was hospitalized.

5723572-3 | Dermatitis Exfoliative, Purpura, Pyrexia, Toxic Skin Eruption, Vasculitis
Adverse event was reported on Apr 22, 2008 by a Female patient taking Fortum (View Usage) (Dosage: ) . Location: FRANCE , 39 years of age, After Fortum was administered, patient had the following side effects: dermatitis exfoliative, purpura, pyrexia, toxic skin eruption, vasculitis (What is vasculitis?). During the same period patient was treated with VANCOMYCIN HCL (View Vancomycin Hcl Review and Vancomycin Hcl Label ), TAZOCILLINE (View Tazocilline Review and Tazocilline Label ), AMIKACIN (View Amikacin Review and Amikacin Label ), FLUCONAZOLE (View Fluconazole Review and Fluconazole Label ), TARGOCID (View Targocid Review and Targocid Label ), AMBISOME (View Ambisome Review and Ambisome Label ), MERONEM (View Meronem Review and Meronem Label ). Patient was hospitalized.

5714624-2 | Oedema Peripheral, Pruritus, Urticaria
on Apr 14, 2008 Male patient from FRANCE , 53 years of age, was diagnosed with wound infection pseudomonas and was treated with Fortum (View Usage). Patient experienced the following unwanted or unexpected effects: oedema peripheral, pruritus, urticaria. Fortum dosage: . During the same period patient was treated with FOSFOCINE (View Fosfocine Review and Fosfocine Label ). Patient was hospitalized.

5704424-1 | Bicytopenia, Neutropenia, Thrombocytopenia
on Apr 02, 2008 Female patient from FRANCE , 68 years of age, was diagnosed with osteitis and was treated with Fortum (View Usage). Patient had the following side effects: bicytopenia, neutropenia, thrombocytopenia. Fortum dosage: . During the same period patient was treated with VANCOMYCIN HCL (View Vancomycin Hcl Review and Vancomycin Hcl Label ), RIFAMPICIN (View Rifampicin Review and Rifampicin Label ), TRIFLUCAN (View Triflucan Review and Triflucan Label ). Patient was hospitalized.

5704423-X | Agitation, Circulatory Collapse, Haemodynamic Instability, Hypotension, Pigmentation Disorder, Pseudomonas Infection, Septic Shock, Somnolence
Patient was taking Fortum (View Usage). After Fortum was administered, patient had the following side effects: agitation, circulatory collapse, haemodynamic instability, hypotension, pigmentation disorder, pseudomonas infection, septic shock, somnolence on Apr 04, 2008 from FRANCE Additional patient health information: Male patient , 68 years of age, was diagnosed with sepsis (What is sepsis?) and. Fortum dosage: 6g Per Day. During the same period patient was treated with VFEND (View Vfend Review and Vfend Label ), COLIMYCINE (10mu Three Times Per Day) (View Colimycine Review and Colimycine Label ), DEROXAT (View Deroxat Review and Deroxat Label ), PREVISCAN (20mg Per Day) (View Previscan Review and Previscan Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), TENORMIN (25mg Three Times Per Day) (View Tenormin Review and Tenormin Label ), TAREG (40mg Per Day) (View Tareg Review and Tareg Label ), ALDACTONE (25mg Per Day) (View Aldactone Review and Aldactone Label ). Patient was hospitalized.

5704419-8 | Purpura
Adverse event was reported on Apr 02, 2008 by a Male patient taking Fortum (View Usage) (Dosage: ) was diagnosed with inflammation, bronchial neoplasm, hyperthermia and. Location: FRANCE , 76 years of age, Patient experienced the following unwanted or unexpected effects: purpura. During the same period patient was treated with ALIMTA (View Alimta Review and Alimta Label ), OFLOCET (View Oflocet Review and Oflocet Label ), ROCEPHIN (View Rocephin Review and Rocephin Label ), TAZOCILLINE (View Tazocilline Review and Tazocilline Label ), CIFLOX (View Ciflox Review and Ciflox Label ). Patient was hospitalized.

5702757-6 | Abdominal Pain, Abdominal Rigidity, Abdominal Symptom, Anuria, Atrial Fibrillation, Blood Creatinine Increased, Cardiomegaly, Cholelithiasis, Clumsiness
on Mar 31, 2008 Female patient from FRANCE , 86 years of age, was diagnosed with urinary tract infection (What is urinary tract infection?) and was treated with Fortum (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), abdominal rigidity, abdominal symptom, anuria, atrial fibrillation (What is atrial fibrillation?), blood creatinine increased, cardiomegaly, cholelithiasis, clumsiness. Fortum dosage: 3g Per Day. During the same period patient was treated with GENTAMICIN (200mg Per Day) (View Gentamicin Review and Gentamicin Label ), LASIX (20mg Per Day) (View Lasix Review and Lasix Label ), CORVASAL (2mg Three Times Per Day) (View Corvasal Review and Corvasal Label ), AMLOR (10mg Per Day) (View Amlor Review and Amlor Label ), ALLOPURINOL (100mg Per Day) (View Allopurinol Review and Allopurinol Label ), XALATAN (1drop Per Day) (View Xalatan Review and Xalatan Label ), COVERSYL (2mg Per Day) (View Coversyl Review and Coversyl Label ), HEMIGOXINE (.125mg Per Day) (View Hemigoxine Review and Hemigoxine Label ). Patient was hospitalized.

5702756-4 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Gamma-glutamyltransferase Increased, Hepatocellular Injury, Liver Function Test Abnormal
on Mar 31, 2008 Female patient from FRANCE , 32 years of age, was diagnosed with wound (What is wound?), renal transplant, type 1 diabetes mellitus and was treated with Fortum (View Usage). After Fortum was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, gamma-glutamyltransferase increased, hepatocellular injury, liver function test abnormal. Fortum dosage: . During the same period patient was treated with CIFLOX (View Ciflox Review and Ciflox Label ), FUCIDINE CAP (View Fucidine Cap Review and Fucidine Cap Label ), NEORAL (200mg Twice Per Day) (View Neoral Review and Neoral Label ), CORTANCYL (5mg Per Day) (View Cortancyl Review and Cortancyl Label ), CELLCEPT (500mg Twice Per Day) (View Cellcept Review and Cellcept Label ), LANTUS (20iu Per Day) (View Lantus Review and Lantus Label ). Patient was hospitalized.

5656989-6 | Balance Disorder, Cerebellar Ataxia, Gait Disturbance, Paresis, Speech Disorder
Patient was taking Fortum (View Usage). Patient experienced the following unwanted or unexpected effects: balance disorder, cerebellar ataxia, gait disturbance, paresis, speech disorder on Feb 29, 2008 from FRANCE Additional patient health information: Male patient , 50 years of age, was diagnosed with brain abscess and. Fortum dosage: . During the same period patient was treated with FLAGYL (500mg Three Times Per Day) (View Flagyl Review and Flagyl Label ), DAFALGAN (View Dafalgan Review and Dafalgan Label ), GARDENAL (View Gardenal Review and Gardenal Label ), ALUMINUM HYDROXIDE AND MAGNESIUM TRISILICATE (View Aluminum Hydroxide And Magnesium Trisilicate Review and Aluminum Hydroxide And Magnesium Trisilicate Label ), DIFFU K (View Diffu K Review and Diffu K Label ). Patient was hospitalized.

5653446-8 | Cholestasis, Effusion, Hepatic Enzyme Increased
Adverse event was reported on Feb 25, 2008 by a Male patient taking Fortum (View Usage) (Dosage: ) was diagnosed with urosepsis and. Location: FRANCE , 51 years of age, Patient had the following side effects: cholestasis, effusion, hepatic enzyme increased. During the same period patient was treated with AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), EFFEXOR (View Effexor Review and Effexor Label ), NOZINAN (View Nozinan Review and Nozinan Label ). Patient was hospitalized.

5647022-0 | Cheilitis, Face Oedema, Lymphadenopathy, Pyrexia, Rash Maculo-papular
on Feb 20, 2008 Male patient from FRANCE , 62 years of age, was diagnosed with febrile bone marrow aplasia and was treated with Fortum (View Usage). After Fortum was administered, patient had the following side effects: cheilitis, face oedema, lymphadenopathy, pyrexia, rash maculo-papular. Fortum dosage: . During the same period patient was treated with VANCOMYCIN HCL (View Vancomycin Hcl Review and Vancomycin Hcl Label ). Patient was hospitalized.

5612626-8 | Acute Pulmonary Oedema, Dizziness, Fatigue, Nervous System Disorder, Overdose, Respiratory Disorder
on Jan 25, 2008 Male patient from FRANCE , 63 years of age, weighting 176.4 lb, was treated with Fortum (View Usage). Patient experienced the following unwanted or unexpected effects: acute pulmonary oedema, dizziness (What is dizziness?), fatigue, nervous system disorder, overdose, respiratory disorder. Fortum dosage: 12g Per Day.

5601291-1 | Anuria, Blood Creatinine Increased, Creatinine Renal Clearance Decreased, Hyponatraemia, Nephritis, Oedema, Renal Failure Acute, Urinary Retention
Patient was taking Fortum (View Usage). Patient had the following side effects: anuria, blood creatinine increased, creatinine renal clearance decreased, hyponatraemia, nephritis, oedema, renal failure acute, urinary retention on Jan 14, 2008 from FRANCE Additional patient health information: Female patient , child 6 years of age, weighting 44.09 lb, was diagnosed with prophylaxis, acute lymphocytic leukaemia, analgesia, abdominal pain (What is abdominal pain?) and. Fortum dosage: 3g Per Day. During the same period patient was treated with ETOPOSIDE (1200mg Per Day) (View Etoposide Review and Etoposide Label ), LARGACTIL (10mg Per Day) (View Largactil Review and Largactil Label ), NUBAIN (4mg Six Times Per Day) (View Nubain Review and Nubain Label ), VOGALENE (20mg Per Day) (View Vogalene Review and Vogalene Label ), SPASFON (View Spasfon Review and Spasfon Label ), PERFALGAN (12g Per Day) (View Perfalgan Review and Perfalgan Label ), DELURSAN (View Delursan Review and Delursan Label ). 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 Fortum 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 Fortum quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Fortum 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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fortum Episodes: 12: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: fosamax Episodes: 1: Diagnosed with major depression.Side ...

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fortum Episodes: 2: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: fosamax Episodes: 1: Diagnosed with major depression.Side ...

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Fortum Reactions
Alanine Aminotransferase Increased
Anaphylactic Reaction
Anuria
Aspartate Aminotransferase Increased
Blood Creatinine Increased
Cholestasis
Confusional State
Convulsion
Death
Dermatitis Exfoliative
Eosinophilia
Erythema
Eschar
Face Oedema
Fungal InfectionWhat is Fungal infection?
Gamma-glutamyltransferase Increased
Hypersensitivity
Neutropenia
Overdose
Pruritus
Pyrexia
RashWhat is Rash?
Rash Maculo-papular
Renal Failure Acute
SepsisWhat is Sepsis?
Skin Exfoliation
Skin Lesion
Thrombocytopenia
Toxic Skin Eruption
Vomiting
Fortum 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 Fortum 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!