VENOFER Side Effects

6266775-4 | Catheter Site Discharge, Catheter Site Swelling
on Jul 09, 2009 Male patient from UNITED STATES , 57 years of age, was diagnosed with anaemia and was treated with Venofer (View Usage). Patient experienced the following unwanted or unexpected effects: catheter site discharge, catheter site swelling. Venofer dosage: 200 Mg.

6266774-2 | Infusion Site Pain, Infusion Site Swelling
Patient was taking Venofer (View Usage). Patient had the following side effects: infusion site pain, infusion site swelling on Jul 09, 2009 from UNITED STATES Additional patient health information: Male patient , 62 years of age, was diagnosed with anaemia and. Venofer dosage: .

6266773-0 | Catheter Site Pain, Ecchymosis
Adverse event was reported on Jul 09, 2009 by a Female patient taking Venofer (View Usage) (Dosage: ) was diagnosed with iron deficiency anaemia and. Location: UNITED STATES , 50 years of age, After Venofer was administered, patient had the following side effects: catheter site pain, ecchymosis.

6266647-5 | Acute Myocardial Infarction, Coronary Artery Occlusion, Coronary Artery Thrombosis, Gastrointestinal Haemorrhage, Renal Infarct, Unresponsive To Stimuli
on Jun 24, 2009 Female patient from UNITED STATES , 66 years of age, weighting 145.0 lb, was diagnosed with iron deficiency anaemia and was treated with Venofer (View Usage). Patient experienced the following unwanted or unexpected effects: acute myocardial infarction, coronary artery occlusion, coronary artery thrombosis, gastrointestinal haemorrhage, renal infarct, unresponsive to stimuli. Venofer dosage: 300mg/m2/week , Intravenous. During the same period patient was treated with FLONASE (View Flonase Review and Flonase Label ), PERCOCET (View Percocet Review and Percocet Label ), ALLEGRA (View Allegra Review and Allegra Label ), NEXIUM (View Nexium Review and Nexium Label ), ADVAIR HFA (View Advair Hfa Review and Advair Hfa Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), ZOLOFT (View Zoloft Review and Zoloft Label ), SPIRIVA (View Spiriva Review and Spiriva Label ). Patient was hospitalized.


6264970-1 | Blood Pressure Immeasurable, Hypotension
on Jul 09, 2009 Female patient from UNITED STATES , 76 years of age, weighting 93.92 lb, was diagnosed with iron deficiency anaemia and was treated with Venofer (View Usage). Patient had the following side effects: blood pressure immeasurable, hypotension. Venofer dosage: 300mg X One Over 90 Min Ivpb. Patient was hospitalized.

6263102-3 | Infusion Site Swelling
Patient was taking Venofer (View Usage). After Venofer was administered, patient had the following side effects: infusion site swelling on Jul 08, 2009 from UNITED STATES Additional patient health information: Female patient , 77 years of age, was diagnosed with anaemia and. Venofer dosage: .

6260941-X | Abdominal Pain, Back Pain, Chromaturia, Diarrhoea, Flank Pain
Adverse event was reported on Jun 16, 2009 by a Female patient taking Venofer (View Usage) (Dosage: 200mg Weekly Intravenous) was diagnosed with iron deficiency anaemia, malabsorption and. Location: UNITED STATES , 29 years of age, weighting 130.0 lb, Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), back pain (What is back pain?), chromaturia, diarrhoea, flank pain.

6243840-9 | Chest Discomfort, Cough, Dyspnoea, Infusion Related Reaction
on Jun 05, 2009 Female patient from SWITZERLAND , 21 years of age, was diagnosed with hypochromic anaemia and was treated with Venofer (View Usage). Patient had the following side effects: chest discomfort, cough, dyspnoea, infusion related reaction. Venofer dosage: 200 Mg In 200ml Ns Intravenous. During the same period patient was treated with FERRIMED (IRON SUCROSE) (View Ferrimed (iron Sucrose) Review and Ferrimed (iron Sucrose) Label ), FERROUS SULFATE TAB (View Ferrous Sulfate Tab Review and Ferrous Sulfate Tab Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ), ADRENALINE (View Adrenaline Review and Adrenaline Label ), MEPYRAMINE (View Mepyramine Review and Mepyramine Label ).

6238227-9 | Infusion Related Reaction, Oedema Peripheral, Pain, Skin Discolouration
on Jun 17, 2009 Female patient from UNITED STATES , 47 years of age, weighting 240.0 lb, was diagnosed with anaemia and was treated with Venofer (View Usage). After Venofer was administered, patient had the following side effects: infusion related reaction, oedema peripheral, pain (What is pain?), skin discolouration. Venofer dosage: 160ml Q 24 Hours Iv.

6231080-9 | Blood Pressure Increased, No Therapeutic Response, Transient Ischaemic Attack, Vitamin B12 Decreased
Patient was taking Venofer (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, no therapeutic response, transient ischaemic attack, vitamin b12 decreased on May 27, 2009 from SWITZERLAND Additional patient health information: Female patient , 76 years of age, . Venofer dosage: 266mg/day Intravenous. During the same period patient was treated with CALCIUM SUPPLEMENT (View Calcium Supplement Review and Calcium Supplement Label ), CORTEF (View Cortef Review and Cortef Label ), DIOVAN (View Diovan Review and Diovan Label ), MIRALAX (View Miralax Review and Miralax Label ), ACULAR LS (EYE DROPS) (KETOROLAC TROMETHAMINE) (View Acular Ls (eye Drops) (ketorolac Tromethamine) Review and Acular Ls (eye Drops) (ketorolac Tromethamine) Label ), PRED FORTE (EYE DROPS) (PREDNISOLONE ACETATE) (View Pred Forte (eye Drops) (prednisolone Acetate) Review and Pred Forte (eye Drops) (prednisolone Acetate) Label ), SENOKOT (SENNOSIDES) (View Senokot (sennosides) Review and Senokot (sennosides) Label ).

6215462-7 | Anaphylactoid Reaction, Dyspnoea, Headache, Hyperhidrosis
Adverse event was reported on May 20, 2009 by a Female patient taking Venofer (View Usage) (Dosage: 300 Mg Weekly) was diagnosed with iron deficiency anaemia and. Location: UNITED STATES , 61 years of age, weighting 180.0 lb, Patient had the following side effects: anaphylactoid reaction, dyspnoea, headache (What is headache?), hyperhidrosis.

6215199-4 | Anaphylactoid Reaction, Dyspnoea, Headache, Hyperhidrosis
on May 20, 2009 Female patient from UNITED STATES , 61 years of age, weighting 180.0 lb, was diagnosed with iron deficiency anaemia and was treated with Venofer (View Usage). After Venofer was administered, patient had the following side effects: anaphylactoid reaction, dyspnoea, headache (What is headache?), hyperhidrosis. Venofer dosage: 300 Mg Weekly.

6215198-2 | Acute Hepatic Failure, Blood Creatinine Increased, Bronchopneumonia, Dyspnoea, Hepatic Encephalopathy, Hepatic Necrosis, Hepatic Siderosis, Hepatotoxicity, Oedema Peripheral
on Mar 20, 2009 Male patient from SWITZERLAND , 86 years of age, weighting 123.5 lb, was diagnosed with iron deficiency anaemia and was treated with Venofer (View Usage). Patient experienced the following unwanted or unexpected effects: acute hepatic failure, blood creatinine increased, bronchopneumonia, dyspnoea, hepatic encephalopathy, hepatic necrosis, hepatic siderosis, hepatotoxicity, oedema peripheral. Venofer dosage: 100mg Twice. During the same period patient was treated with INJECTAFER (FERRIC CARBOXYMALTOSE) (500 Mg Twice) (View Injectafer (ferric Carboxymaltose) Review and Injectafer (ferric Carboxymaltose) Label ), SALBUTAMOL SULFATE (View Salbutamol Sulfate Review and Salbutamol Sulfate Label ), BUDESONIDUM (View Budesonidum Review and Budesonidum Label ), IPRATROPII BROMIDUM (View Ipratropii Bromidum Review and Ipratropii Bromidum Label ), FUROSEMID (View Furosemid Review and Furosemid Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), EPOETIN BETA (View Epoetin Beta Review and Epoetin Beta Label ), VALSARTAN (View Valsartan Review and Valsartan Label ).

6215192-1 | Dyspnoea, Hypocapnia, Hypoxia
Patient was taking Venofer (View Usage). Patient had the following side effects: dyspnoea, hypocapnia, hypoxia on May 22, 2009 from SWITZERLAND Additional patient health information: Female patient , 72 years of age, was diagnosed with anaemia postoperative and. Venofer dosage: 300 Mg/day Intravenous.

6215181-7 | Lymphadenopathy, Lymphocytosis, Pyrexia
Adverse event was reported on May 20, 2009 by a Male patient taking Venofer (View Usage) (Dosage: 400 Mg Intravenous) . Location: SWITZERLAND , 78 years of age, After Venofer was administered, patient had the following side effects: lymphadenopathy, lymphocytosis, pyrexia. During the same period patient was treated with ROCEPHIN (View Rocephin Review and Rocephin Label ), FLAGYL (View Flagyl Review and Flagyl Label ), RED BLOOD CELL TRANSFUSION (View Red Blood Cell Transfusion Review and Red Blood Cell Transfusion Label ). Patient was hospitalized.

6212354-4 | Rhabdomyolysis
on May 14, 2009 Male patient from SWITZERLAND , weighting 44.09 lb, was treated with Venofer (View Usage). Patient experienced the following unwanted or unexpected effects: rhabdomyolysis. Venofer dosage: 100mg, 2 Administrations Intravenous. During the same period patient was treated with PARACETAMOL (View Paracetamol Review and Paracetamol Label ), KETAMINE HCL (View Ketamine Hcl Review and Ketamine Hcl Label ), HEPARIN (View Heparin Review and Heparin Label ). Patient was hospitalized.

6212232-0 | Pruritus, Urticaria
on May 13, 2009 Female patient from UNITED STATES , 61 years of age, was diagnosed with renal failure chronic and was treated with Venofer (View Usage). Patient had the following side effects: pruritus, urticaria. Venofer dosage: 100 Mg On 2 Occasions Intravenous. During the same period patient was treated with EPOGEN (View Epogen Review and Epogen Label ). Patient was hospitalized.

6205954-9 | Extravasation, Skin Discolouration, Skin Disorder
Patient was taking Venofer (View Usage). After Venofer was administered, patient had the following side effects: extravasation, skin discolouration, skin disorder on May 27, 2009 from UNITED STATES Additional patient health information: Female patient , 55 years of age, weighting 108.0 lb, was diagnosed with anaemia and. Venofer dosage: 200 Mg Daily Iv.

6204442-3 | Acute Hepatic Failure, Blood Creatinine Increased, Body Temperature Increased, Bronchopneumonia, Dyspnoea, Hepatic Encephalopathy, Hepatic Necrosis, Oedema Peripheral, Right Ventricular Failure
Adverse event was reported on Mar 20, 2009 by a Male patient taking Venofer (View Usage) (Dosage: 100mg Twice/11/9 And 12, 2008) was diagnosed with iron deficiency anaemia and. Location: SWITZERLAND , 86 years of age, weighting 123.5 lb, Patient experienced the following unwanted or unexpected effects: acute hepatic failure, blood creatinine increased, body temperature increased, bronchopneumonia, dyspnoea, hepatic encephalopathy, hepatic necrosis, oedema peripheral, right ventricular failure. During the same period patient was treated with INJECTAFER (FERRIC CARBOXYMALTOSE) (500 Mg Once) (View Injectafer (ferric Carboxymaltose) Review and Injectafer (ferric Carboxymaltose) Label ), SALBUTAMOL SULFATE (View Salbutamol Sulfate Review and Salbutamol Sulfate Label ), BUDESONIDUM (View Budesonidum Review and Budesonidum Label ), IPRATROPIL BROMIDUM (View Ipratropil Bromidum Review and Ipratropil Bromidum Label ), FUROSEMID (View Furosemid Review and Furosemid Label ).

6204395-8 | Blood Pressure Increased, Cardiomegaly, Emphysema, No Therapeutic Response, Transient Ischaemic Attack, Treatment Noncompliance
on May 08, 2009 Female patient from SWITZERLAND , 76 years of age, was treated with Venofer (View Usage). Patient had the following side effects: blood pressure increased, cardiomegaly, emphysema, no therapeutic response, transient ischaemic attack, treatment noncompliance. Venofer dosage: 266mg/day Intravenous. During the same period patient was treated with CALCIUM SUPPLEMENT (View Calcium Supplement Review and Calcium Supplement Label ), CORTEF (View Cortef Review and Cortef Label ), DIOVAN (View Diovan Review and Diovan Label ), FENTANYL (FENTANYL (BUCCAL)) (View Fentanyl (fentanyl (buccal)) Review and Fentanyl (fentanyl (buccal)) Label ), NITROQUICK (NITROGLYCERIN) (View Nitroquick (nitroglycerin) Review and Nitroquick (nitroglycerin) Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ), PROTONIX (PANTOPRAXOLE SODIUM) (View Protonix (pantopraxole Sodium) Review and Protonix (pantopraxole Sodium) Label ). Patient was hospitalized.

6194944-0 | Anaphylactic Shock, Unresponsive To Stimuli
on May 15, 2009 Female patient from UNITED STATES , 40 years of age, weighting 157.0 lb, was diagnosed with deficiency anaemia and was treated with Venofer (View Usage). After Venofer was administered, patient had the following side effects: anaphylactic shock, unresponsive to stimuli. Venofer dosage: . Patient was hospitalized.

6193465-9 | Infusion Site Extravasation
Patient was taking Venofer (View Usage). Patient experienced the following unwanted or unexpected effects: infusion site extravasation on May 14, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 115.1 lb, was diagnosed with anaemia and. Venofer dosage: 300 Mg Qam X 1 Dose Iv Drip.

6189362-5 | Feeling Hot, Hypotension, Injection Site Pain, Joint Stiffness, Loss Of Consciousness, Musculoskeletal Stiffness, Nausea, Skin Discolouration, Syncope
Adverse event was reported on Apr 24, 2009 by a Female patient taking Venofer (View Usage) (Dosage: 500 Mg In 100 Ml Ns, Intravenous) was diagnosed with anaemia and. Location: UNITED STATES , 61 years of age, Patient had the following side effects: feeling hot, hypotension, injection site pain, joint stiffness, loss of consciousness, musculoskeletal stiffness, nausea (What is nausea?), skin discolouration, syncope.

6188758-5 | Chest Pain, Headache, Hypertension, Infusion Related Reaction
on May 11, 2009 Female patient from UNITED STATES , 74 years of age, weighting 209.4 lb, was diagnosed with anaemia and was treated with Venofer (View Usage). After Venofer was administered, patient had the following side effects: chest pain (What is chest pain?), headache (What is headache?), hypertension, infusion related reaction. Venofer dosage: 400mg Once Iv.

6185781-1 | Phlebitis
on Apr 23, 2009 Female patient from UNITED STATES , 59 years of age, weighting 155.0 lb, was diagnosed with iron deficiency anaemia and was treated with Venofer (View Usage). Patient experienced the following unwanted or unexpected effects: phlebitis. Venofer dosage: See Image.

6185779-3 | Injection Site Streaking, Phlebitis
Patient was taking Venofer (View Usage). Patient had the following side effects: injection site streaking, phlebitis on Apr 23, 2009 from Additional patient health information: Female patient , 62 years of age, weighting 176.0 lb, was diagnosed with iron deficiency anaemia and. Venofer dosage: 100 Mg/100 Ml Ns/qd.

6170932-5 | Infusion Site Extravasation
Adverse event was reported on Apr 28, 2009 by a Female patient taking Venofer (View Usage) (Dosage: 300mg Once Iv) was diagnosed with anaemia and. Location: UNITED STATES , 48 years of age, weighting 103.6 lb, After Venofer was administered, patient had the following side effects: infusion site extravasation.

6169292-5 | Injection Site Pain, Injection Site Reaction, Injection Site Streaking, Phlebitis
on Apr 10, 2009 Female patient from UNITED STATES , 58 years of age, weighting 131.0 lb, was diagnosed with iron deficiency anaemia and was treated with Venofer (View Usage). Patient experienced the following unwanted or unexpected effects: injection site pain, injection site reaction, injection site streaking, phlebitis. Venofer dosage: 200 Mg Intravenous. During the same period patient was treated with LEVAQUIN (View Levaquin Review and Levaquin Label ).

6168939-7 | Blood Pressure Increased, Flushing, Pruritus, Respiratory Rate Increased, Skin Tightness
on Apr 24, 2009 Female patient from UNITED STATES , weighting 267.0 lb, was diagnosed with iron deficiency, menorrhagia and was treated with Venofer (View Usage). Patient had the following side effects: blood pressure increased, flushing, pruritus, respiratory rate increased, skin tightness. Venofer dosage: 333 Mg X 3 Doses Iv Drip.

6166484-6 | Atelectasis, Bronchitis, Haematemesis, Haemoptysis, Lung Neoplasm
Patient was taking Venofer (View Usage). After Venofer was administered, patient had the following side effects: atelectasis, bronchitis (What is bronchitis?), haematemesis, haemoptysis, lung neoplasm on Apr 16, 2009 from CANADA Additional patient health information: Female patient , 58 years of age, . Venofer dosage: Unk. During the same period patient was treated with SALBUTAMOL (Unk) (View Salbutamol Review and Salbutamol Label ), RENAGEL (Unk) (View Renagel Review and Renagel Label ), PYRIDOXINE (Unk) (View Pyridoxine Review and Pyridoxine Label ), NORVASC (Unk) (View Norvasc Review and Norvasc Label ), LYRICA (Unk) (View Lyrica Review and Lyrica Label ), FUROSEMIDE (Unk) (View Furosemide Review and Furosemide Label ), CLONAZEPAM (Unk) (View Clonazepam Review and Clonazepam Label ), CALCIUM CARBONATE (Unk) (View Calcium Carbonate Review and Calcium Carbonate Label ).

6161957-4 | Anxiety, Apnoea, Body Temperature Decreased, Chest Discomfort, Loss Of Consciousness, Movement Disorder, Nausea, Oedema Peripheral, Paraesthesia
Adverse event was reported on Apr 17, 2009 by a Female patient taking Venofer (View Usage) (Dosage: 333 Mg Once Iv Drip) was diagnosed with anaemia and. Location: UNITED STATES , 41 years of age, weighting 149.0 lb, Patient experienced the following unwanted or unexpected effects: anxiety (What is anxiety?), apnoea, body temperature decreased, chest discomfort, loss of consciousness, movement disorder (What is movement disorder?), nausea (What is nausea?), oedema peripheral, paraesthesia.

6161773-3 | Agitation, Apnoea, Chest Discomfort, Dyskinesia, Nausea, Oedema Peripheral, Unresponsive To Stimuli, Urticaria
on Apr 17, 2009 Female patient from UNITED STATES , 41 years of age, weighting 149.0 lb, was diagnosed with iron deficiency anaemia and was treated with Venofer (View Usage). Patient had the following side effects: agitation, apnoea, chest discomfort, dyskinesia, nausea (What is nausea?), oedema peripheral, unresponsive to stimuli, urticaria. Venofer dosage: 333 Mg Weekly Iv, Over 1 Hour. Patient was hospitalized.

6160318-1 | Ecchymosis, Extravasation
on Apr 02, 2009 Female patient from UNITED STATES , 71 years of age, weighting 174.0 lb, was treated with Venofer (View Usage). After Venofer was administered, patient had the following side effects: ecchymosis, extravasation. Venofer dosage: 200mg In 100ml Fuild/60 Min Intravenous. Patient was hospitalized.

6159320-5 | C-reactive Protein Increased, Haemoglobin Decreased, Induced Labour, Malaise, Platelet Count Decreased, Premature Rupture Of Membranes
Patient was taking Venofer (View Usage). Patient experienced the following unwanted or unexpected effects: c-reactive protein increased, haemoglobin decreased, induced labour, malaise, platelet count decreased, premature rupture of membranes on Apr 02, 2009 from SWITZERLAND Additional patient health information: Female patient , 25 years of age, was diagnosed with haemoglobin decreased and. Venofer dosage: 20 Mg/ml Intravenous. During the same period patient was treated with FERROUS SULFATE TAB (View Ferrous Sulfate Tab Review and Ferrous Sulfate Tab Label ).

6154056-9 | Pruritus, Urticaria
Adverse event was reported on Mar 31, 2009 by a Female patient taking Venofer (View Usage) (Dosage: 100 Mg On 2 Occasions, Intravenous) was diagnosed with renal failure chronic and. Location: UNITED STATES , 61 years of age, Patient had the following side effects: pruritus, urticaria. During the same period patient was treated with EPOGEN (View Epogen Review and Epogen Label ). Patient was hospitalized.

6153943-5 | Catheter Related Complication, Pleural Effusion
on Mar 26, 2009 Female patient from UNITED STATES , 65 years of age, weighting 189.8 lb, was diagnosed with iron deficiency anaemia, anaesthesia and was treated with Venofer (View Usage). After Venofer was administered, patient had the following side effects: catheter related complication, pleural effusion. Venofer dosage: 200mg/day X 3 Days, Intravenous. During the same period patient was treated with PROPOFOL (Intravenous; Route: Drip) (View Propofol Review and Propofol Label ), MORPHINE (View Morphine Review and Morphine Label ), PROPOXYPHENE HCL CAP (View Propoxyphene Hcl Cap Review and Propoxyphene Hcl Cap Label ), HEP FLUSH (View Hep Flush Review and Hep Flush Label ), ROCEPHIN (View Rocephin Review and Rocephin Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), CALCIUM CARBONATE (View Calcium Carbonate Review and Calcium Carbonate Label ). Patient was hospitalized.

6152156-0 | Dehydration, Hypotension, Hypoxia, Sepsis, Syncope
on Apr 09, 2009 Male patient from UNITED STATES , weighting 146.3 lb, was diagnosed with anaemia and was treated with Venofer (View Usage). Patient experienced the following unwanted or unexpected effects: dehydration, hypotension, hypoxia, sepsis (What is sepsis?), syncope. Venofer dosage: 300mg One Time Iv Drip. Patient was hospitalized.

6146633-6 | Infusion Related Reaction, Malaise, Muscle Rigidity, Pain
Patient was taking Venofer (View Usage). Patient had the following side effects: infusion related reaction, malaise, muscle rigidity, pain (What is pain?) on Apr 03, 2009 from UNITED STATES Additional patient health information: Male patient , 59 years of age, weighting 140.0 lb, was diagnosed with anaemia and. Venofer dosage: 200 Mg Qday Iv. During the same period patient was treated with ZANTAC (View Zantac Review and Zantac Label ), ATIVAN (View Ativan Review and Ativan Label ), MORPHINE (View Morphine Review and Morphine Label ), INTRALIPIDS (View Intralipids Review and Intralipids Label ), TPN (View Tpn Review and Tpn Label ), LASIX (View Lasix Review and Lasix Label ), ADVAIR HFA (View Advair Hfa Review and Advair Hfa Label ), DUONEB (View Duoneb Review and Duoneb Label ).

6142477-X | Asthenia, Nausea, Pallor, Rash
Adverse event was reported on Apr 01, 2009 by a Female patient taking Venofer (View Usage) (Dosage: 500 Mg Iv X 1) was diagnosed with anaemia and. Location: UNITED STATES , 88 years of age, weighting 142.0 lb, After Venofer was administered, patient had the following side effects: asthenia, nausea (What is nausea?), pallor, rash (What is rash?). Patient was hospitalized.

6142257-5 | Dyspnoea, Oedema Peripheral, Urticaria
on Apr 01, 2009 Female patient from UNITED STATES , 27 years of age, weighting 132.0 lb, was diagnosed with anaemia and was treated with Venofer (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, oedema peripheral, urticaria. Venofer dosage: 500 Mg Iv X 1. Patient was hospitalized.

6140492-3 | Inflammation, Renal Infarct
on Mar 17, 2009 Female patient from UNITED STATES , 66 years of age, weighting 145.0 lb, was diagnosed with iron deficiency anaemia, menopause (What is menopause?) and was treated with Venofer (View Usage). Patient had the following side effects: inflammation, renal infarct. Venofer dosage: 300 Mg/m2/week, 20 Mg/ml; Intravenous. During the same period patient was treated with PREMPRO (0.3mg/day Oral) (View Prempro Review and Prempro Label ), FLONASE (View Flonase Review and Flonase Label ), PERCOCET (View Percocet Review and Percocet Label ), ALLEGRA (View Allegra Review and Allegra Label ), NEXIUM (View Nexium Review and Nexium Label ), ADVAIR HFA (View Advair Hfa Review and Advair Hfa Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), ZOLOFT (View Zoloft Review and Zoloft Label ). Patient was hospitalized.

6139622-9 | Infusion Related Reaction, Malaise, Muscle Rigidity, Pain
Patient was taking Venofer (View Usage). After Venofer was administered, patient had the following side effects: infusion related reaction, malaise, muscle rigidity, pain (What is pain?) on Mar 31, 2009 from UNITED STATES Additional patient health information: Male patient , 59 years of age, weighting 140.0 lb, was diagnosed with anaemia and. Venofer dosage: 200 Mg Q Day Iv. During the same period patient was treated with ZANTAC (View Zantac Review and Zantac Label ), ATIVAN (View Ativan Review and Ativan Label ), MORPHINE (View Morphine Review and Morphine Label ), INTRALIPIDS (View Intralipids Review and Intralipids Label ), TPN (View Tpn Review and Tpn Label ), LASIX (View Lasix Review and Lasix Label ), ADVAIR HFA (View Advair Hfa Review and Advair Hfa Label ), DUONEB (View Duoneb Review and Duoneb Label ).

6138779-3 | Loss Of Consciousness, Malaise, Mydriasis
Adverse event was reported on Mar 17, 2009 by a Female patient taking Venofer (View Usage) (Dosage: 300 Mg Intravenous) was diagnosed with anaemia and. Location: SWITZERLAND , 55 years of age, Patient experienced the following unwanted or unexpected effects: loss of consciousness, malaise, mydriasis. During the same period patient was treated with TEGRETOL (CARBAMAZEPIN) (View Tegretol (carbamazepin) Review and Tegretol (carbamazepin) Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), BISOPROLOL FUMARATE (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), INEXIM (ESOMEPRAZOL) (View Inexim (esomeprazol) Review and Inexim (esomeprazol) Label ), LIORESAL (View Lioresal Review and Lioresal Label ), LAROXYL (AMITRIPTYLIN) (View Laroxyl (amitriptylin) Review and Laroxyl (amitriptylin) Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ).

6137884-5 | Body Temperature Increased, Chest Pain, Erythema, Flushing, Infusion Related Reaction, Paraesthesia
on Mar 13, 2009 Female patient from UNITED STATES , 74 years of age, weighting 150.0 lb, was diagnosed with iron deficiency anaemia and was treated with Venofer (View Usage). Patient had the following side effects: body temperature increased, chest pain (What is chest pain?), erythema, flushing, infusion related reaction, paraesthesia. Venofer dosage: 200 Mg Intravenous.

6137651-2 | Dyspnoea
on Mar 27, 2009 Female patient from UNITED STATES , 65 years of age, weighting 86.10 lb, was diagnosed with iron deficiency anaemia, anaesthesia and was treated with Venofer (View Usage). After Venofer was administered, patient had the following side effects: dyspnoea. Venofer dosage: 200 Mg Daily X 3 Iv Drip. During the same period patient was treated with PROPOFOL (Unsure Unsure Iv Drip) (View Propofol Review and Propofol Label ), MORPHINE (View Morphine Review and Morphine Label ), PROPOXYPHENE HCL CAP (View Propoxyphene Hcl Cap Review and Propoxyphene Hcl Cap Label ), HEP FLUASH (View Hep Fluash Review and Hep Fluash Label ), ROCEPHIN (View Rocephin Review and Rocephin Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), CALCIUM CARONATE (View Calcium Caronate Review and Calcium Caronate Label ).

6128750-X | Erythema Multiforme
Patient was taking Venofer (View Usage). Patient experienced the following unwanted or unexpected effects: erythema multiforme on Mar 05, 2009 from SWITZERLAND Additional patient health information: Female patient , 35 years of age, was diagnosed with iron deficiency and. Venofer dosage: 200 Mg (100mg, 2x's Day) Intravenous.

6108687-2 | Abdominal Discomfort, Anaphylactoid Reaction, Bradycardia, Burning Sensation, Hypotension, Hypovolaemia, Infusion Related Reaction, Infusion Site Urticaria, Nausea
Adverse event was reported on Feb 13, 2009 by a Female patient taking Venofer (View Usage) (Dosage: 300mg; Intravenous, 20 Mg/ml) was diagnosed with iron deficiency anaemia and. Location: SWITZERLAND , 49 years of age, Patient had the following side effects: abdominal discomfort, anaphylactoid reaction, bradycardia, burning sensation, hypotension, hypovolaemia, infusion related reaction, infusion site urticaria, nausea (What is nausea?). During the same period patient was treated with TAVEGYL (Dosage) (View Tavegyl Review and Tavegyl Label ), BELOK ZOK (METOPROLOL) (View Belok Zok (metoprolol) Review and Belok Zok (metoprolol) Label ), LISITRIL (LISINOPRIL) (View Lisitril (lisinopril) Review and Lisitril (lisinopril) Label ), ESTROGEN/PROGESTERONE (View Estrogen/progesterone Review and Estrogen/progesterone Label ).

6094478-8 | Erythema, Injection Site Phlebitis, Venous Thrombosis Limb
on Feb 06, 2009 Male patient from SWITZERLAND , 39 years of age, was diagnosed with iron deficiency anaemia and was treated with Venofer (View Usage). After Venofer was administered, patient had the following side effects: erythema, injection site phlebitis, venous thrombosis limb. Venofer dosage: Intravenous Drip. During the same period patient was treated with ATRIXTRA (FONDAPARINUX) (View Atrixtra (fondaparinux) Review and Atrixtra (fondaparinux) Label ), FERROSTRANE (FERRIC SODIUM EDETATE) (View Ferrostrane (ferric Sodium Edetate) Review and Ferrostrane (ferric Sodium Edetate) Label ), PERFALGAN (PARACETAMOL) (View Perfalgan (paracetamol) Review and Perfalgan (paracetamol) Label ), TOPALGIC (TRAMADOL) (View Topalgic (tramadol) Review and Topalgic (tramadol) Label ), AUGMENTIN (AMOXICILLIN, CLAVULANIC ACID) (View Augmentin (amoxicillin, Clavulanic Acid) Review and Augmentin (amoxicillin, Clavulanic Acid) Label ). Patient was hospitalized.

6094477-6 | Extravasation, Infusion Site Abscess
on Feb 05, 2009 Female patient from SWITZERLAND , 35 years of age, was diagnosed with anaemia postoperative and was treated with Venofer (View Usage). Patient experienced the following unwanted or unexpected effects: extravasation, infusion site abscess. Venofer dosage: 100 Mg Intravenous.

6094441-7 | Infusion Site Extravasation, Infusion Site Reaction, Infusion Site Swelling, Thrombophlebitis
Patient was taking Venofer (View Usage). Patient had the following side effects: infusion site extravasation, infusion site reaction, infusion site swelling, thrombophlebitis on Feb 05, 2009 from SOUTH AFRICA Additional patient health information: Male patient , 76 years of age, was diagnosed with iron deficiency anaemia and. Venofer dosage: 200 Mg, 4 Infusions Intravenous Drip. During the same period patient was treated with PERINDOPRIL ERBUMINE (View Perindopril Erbumine Review and Perindopril Erbumine Label ), CARLOC (CARVEDILOL) (View Carloc (carvedilol) Review and Carloc (carvedilol) Label ), ALLERGEX (CHLORPHENIRAMINE MALEATE) (View Allergex (chlorpheniramine Maleate) Review and Allergex (chlorpheniramine Maleate) Label ), SINUCON (OHENYTOLOXAMINE CITRATE, CHLORPHENIRAMINE MALEATED, PHENYLEPH (View Sinucon (ohenytoloxamine Citrate, Chlorpheniramine Maleated, Phenyleph Review and Sinucon (ohenytoloxamine Citrate, Chlorpheniramine Maleated, Phenyleph Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.