RANIPLEX Side Effects

6488219-X | Anaemia, Device Related Infection, Neutropenia, Pyrexia
on Dec 02, 2009 Male patient from FRANCE , weighting 9.70 lb, was treated with Raniplex (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, device related infection, neutropenia, pyrexia. Raniplex dosage: . During the same period patient was treated with VANCOMYCIN (View Vancomycin Review and Vancomycin Label ), AMIKLIN (View Amiklin Review and Amiklin Label ), CLAFORAN (View Claforan Review and Claforan Label ). Patient was hospitalized.

6470771-1 | Anaemia, Device Related Infection, Neutropenia, Pyrexia
Patient was taking Raniplex (View Usage). Patient had the following side effects: anaemia, device related infection, neutropenia, pyrexia on Nov 23, 2009 from FRANCE Additional patient health information: Male patient , weighting 9.70 lb, . Raniplex dosage: . During the same period patient was treated with VANCOMYCIN (View Vancomycin Review and Vancomycin Label ), AMIKLIN (View Amiklin Review and Amiklin Label ), CLAFORAN (View Claforan Review and Claforan Label ). Patient was hospitalized.

6074130-5 | Gastrooesophageal Reflux Disease, Necrotising Colitis, Regurgitation
Adverse event was reported on Feb 10, 2009 by a Male patient taking Raniplex (View Usage) (Dosage: 10mgkd Twice Per Day) . Location: FRANCE , weighting 4.41 lb, After Raniplex was administered, patient had the following side effects: gastrooesophageal reflux disease, necrotising colitis, regurgitation. Patient was hospitalized.

6048486-3 | Blood Bilirubin Increased, Headache, Hepatocellular Injury, Leukopenia, Malaise, Nausea, Neutropenia, Platelet Count Decreased, Vertigo
on Jan 15, 2009 Male patient from FRANCE , 53 years of age, was diagnosed with mycobacterium marinum infection and was treated with Raniplex (View Usage). Patient experienced the following unwanted or unexpected effects: blood bilirubin increased, headache (What is headache?), hepatocellular injury, leukopenia, malaise, nausea (What is nausea?), neutropenia, platelet count decreased, vertigo. Raniplex dosage: . During the same period patient was treated with MINOCYCLINE HCL (View Minocycline Hcl Review and Minocycline Hcl Label ), ULTRA LEVURE (View Ultra Levure Review and Ultra Levure Label ). Patient was hospitalized.


5872112-7 | Blood Bilirubin Increased, Headache, Hepatocellular Injury, Leukopenia, Malaise, Nausea, Neutropenia, Vertigo
on Sep 04, 2008 Male patient from FRANCE , 53 years of age, was diagnosed with mycobacterium marinum infection and was treated with Raniplex (View Usage). Patient had the following side effects: blood bilirubin increased, headache (What is headache?), hepatocellular injury, leukopenia, malaise, nausea (What is nausea?), neutropenia, vertigo. Raniplex dosage: . During the same period patient was treated with MINOCYCLINE HCL (View Minocycline Hcl Review and Minocycline Hcl Label ), ULTRA LEVURE (View Ultra Levure Review and Ultra Levure Label ). Patient was hospitalized.

5804481-8 | Abortion Induced, Gestational Diabetes
Patient was taking Raniplex (View Usage). After Raniplex was administered, patient had the following side effects: abortion induced, gestational diabetes on Jul 03, 2008 from FRANCE Additional patient health information: Female patient , 40 years of age, . Raniplex dosage: . During the same period patient was treated with ALDACTONE (75mg Per Day) (View Aldactone Review and Aldactone Label ), ZOLOFT (50mg Per Day) (View Zoloft Review and Zoloft Label ), LYSANXIA (View Lysanxia Review and Lysanxia Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).

5800506-4 | Abortion Induced, Gestational Diabetes
Adverse event was reported on Jun 27, 2008 by a Female patient taking Raniplex (View Usage) (Dosage: ) . Location: FRANCE , 40 years of age, Patient experienced the following unwanted or unexpected effects: abortion induced, gestational diabetes. During the same period patient was treated with ALDACTONE (75mg Per Day) (View Aldactone Review and Aldactone Label ), ZOLOFT (50mg Per Day) (View Zoloft Review and Zoloft Label ), LYSANXIA (View Lysanxia Review and Lysanxia Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).

5771874-7 | Blood Disorder, Gastrointestinal Disorder, Nervous System Disorder, Neuralgia, Pruritus, Rash Erythematous, Skin Exfoliation
on Jun 09, 2008 Female patient from FRANCE , 61 years of age, was diagnosed with ascites and was treated with Raniplex (View Usage). Patient had the following side effects: blood disorder, gastrointestinal disorder, nervous system disorder, neuralgia, pruritus, rash erythematous, skin exfoliation. Raniplex dosage: . During the same period patient was treated with TAXOL (View Taxol Review and Taxol Label ), KYTRIL (View Kytril Review and Kytril Label ), CORDARONE (View Cordarone Review and Cordarone Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), SECTRAL (View Sectral Review and Sectral Label ), CARBOPLATIN (View Carboplatin Review and Carboplatin Label ), MORPHINE (View Morphine Review and Morphine Label ).

5759790-8 | Blood Disorder, Gastrointestinal Disorder, Nervous System Disorder, Neuralgia, Pruritus, Rash Erythematous, Skin Exfoliation
on Jun 03, 2008 Female patient from FRANCE , 61 years of age, was diagnosed with ascites and was treated with Raniplex (View Usage). After Raniplex was administered, patient had the following side effects: blood disorder, gastrointestinal disorder, nervous system disorder, neuralgia, pruritus, rash erythematous, skin exfoliation. Raniplex dosage: . During the same period patient was treated with TAXOL (View Taxol Review and Taxol Label ), KYTRIL (View Kytril Review and Kytril Label ), CORDARONE (View Cordarone Review and Cordarone Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), SECTRAL (View Sectral Review and Sectral Label ), CARBOPLATIN (View Carboplatin Review and Carboplatin Label ), MORPHINE (View Morphine Review and Morphine Label ).

5717990-7 | Anaemia Haemolytic Autoimmune, Dyspnoea, Melanosis Coli
Patient was taking Raniplex (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia haemolytic autoimmune, dyspnoea, melanosis coli on Apr 11, 2008 from FRANCE Additional patient health information: Male patient , 57 years of age, was diagnosed with gastrooesophageal reflux disease and. Raniplex dosage: 300mg Per Day.

5612627-X | Chest Discomfort, Chest Pain, Dyspnoea, Myocardial Infarction, Tachycardia, Troponin Increased
Adverse event was reported on Jan 22, 2008 by a Male patient taking Raniplex (View Usage) (Dosage: 50mg Per Day) . Location: FRANCE , 70 years of age, Patient had the following side effects: chest discomfort, chest pain (What is chest pain?), dyspnoea, myocardial infarction, tachycardia, troponin increased. During the same period patient was treated with SOLU MEDROL (120mg Per Day) (View Solu-medrol Review and Solu-medrol Label ), TAXOTERE (30mg Per Day) (View Taxotere Review and Taxotere Label ), KYTRIL (3mg Per Day) (View Kytril Review and Kytril Label ), POLARAMINE (5mg Per Day) (View Polaramine Review and Polaramine Label ). Patient was hospitalized.

5594799-9 | Anaemia Haemolytic Autoimmune
on Jan 11, 2008 Male patient from FRANCE , 57 years of age, was treated with Raniplex (View Usage). After Raniplex was administered, patient had the following side effects: anaemia haemolytic autoimmune. Raniplex dosage: 300mg Per Day.

5574987-8 | Anaemia Haemolytic Autoimmune
on Dec 20, 2007 Male patient from FRANCE , 57 years of age, was treated with Raniplex (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia haemolytic autoimmune. Raniplex dosage: .

5525573-7 | Anaphylactic Shock, Convulsion, Hypotension, Loss Of Consciousness
Patient was taking Raniplex (View Usage). Patient had the following side effects: anaphylactic shock, convulsion, hypotension, loss of consciousness on Nov 21, 2007 from FRANCE Additional patient health information: Male patient , 54 years of age, . Raniplex dosage: 1unit Per Day. During the same period patient was treated with CETUXIMAB (View Cetuximab Review and Cetuximab Label ), OSMOTAN (View Osmotan Review and Osmotan Label ), PRIMPERAN INJ (1unit Per Day) (View Primperan Inj Review and Primperan Inj Label ), POLARAMINE (1unit Per Day) (View Polaramine Review and Polaramine Label ), SOLU MEDROL (80mg Per Day) (View Solu-medrol Review and Solu-medrol Label ), FOLINIC ACID (View Folinic Acid Review and Folinic Acid Label ), OXALIPLATIN (View Oxaliplatin Review and Oxaliplatin Label ), FLUOROURACIL (View Fluorouracil Review and Fluorouracil Label ). Patient was hospitalized.

5358902-8 | Eosinophilia, Pruritus
Adverse event was reported on Jun 08, 2007 by a Male patient taking Raniplex (View Usage) (Dosage: 50mg Per Day) . Location: FRANCE , 68 years of age, After Raniplex was administered, patient had the following side effects: eosinophilia, pruritus. During the same period patient was treated with PARACETAMOL (View Paracetamol Review and Paracetamol Label ), FRAXIPARINE (View Fraxiparine Review and Fraxiparine Label ), SPASFON (View Spasfon Review and Spasfon Label ). Patient was hospitalized.

5290652-9 | Pemphigoid
on Mar 30, 2007 Female patient from FRANCE , 83 years of age, was diagnosed with erysipelas and was treated with Raniplex (View Usage). Patient experienced the following unwanted or unexpected effects: pemphigoid. Raniplex dosage: 150mg Per Day. During the same period patient was treated with DIANTALVIC (View Diantalvic Review and Diantalvic Label ), PYOSTACINE (View Pyostacine Review and Pyostacine Label ), ISOSORBIDE MONONITRATE (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ), ZESTRIL (View Zestril Review and Zestril Label ), LOVENOX (View Lovenox Review and Lovenox Label ). Patient was hospitalized.

5135430-6 | Deep Vein Thrombosis, Dyspnoea, Phlebitis, Pulmonary Embolism
on Oct 16, 2006 Male patient from FRANCE , 65 years of age, weighting 154.3 lb, was diagnosed with colon cancer metastatic and was treated with Raniplex (View Usage). Patient had the following side effects: deep vein thrombosis (What is deep vein thrombosis?), dyspnoea, phlebitis, pulmonary embolism (What is pulmonary embolism?). Raniplex dosage: 50mg Cyclic. During the same period patient was treated with FRAXODI (View Fraxodi Review and Fraxodi Label ), ZOFRAN (View Zofran Review and Zofran Label ), DEXAMETHASONE 4MG TAB (20mg Cyclic) (View Dexamethasone 4mg Tab Review and Dexamethasone 4mg Tab Label ), CAMPTOSAR (180mg Cyclic) (View Camptosar Review and Camptosar Label ), CETUXIMAB (250mg Cyclic) (View Cetuximab Review and Cetuximab Label ), POLARAMINE (View Polaramine Review and Polaramine Label ), ATROPINE (View Atropine Review and Atropine Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ). Patient was hospitalized.

5135429-X | Confusional State, Dermatitis Exfoliative, Dizziness Postural, Eosinophilia, Erythema, Gamma-glutamyltransferase Increased, Hepatitis, Hypersensitivity
Patient was taking Raniplex (View Usage). After Raniplex was administered, patient had the following side effects: confusional state, dermatitis exfoliative, dizziness postural, eosinophilia, erythema, gamma-glutamyltransferase increased, hepatitis (What is hepatitis?), hypersensitivity on Oct 16, 2006 from FRANCE Additional patient health information: Female patient , 48 years of age, was diagnosed with nephrotic syndrome and. Raniplex dosage: . During the same period patient was treated with CORTICOID (20mg Per Day) (View Corticoid Review and Corticoid Label ). Patient was hospitalized.

5134647-4 | Coma Acidotic, Thrombocytopenia
Adverse event was reported on Oct 16, 2006 by a Male patient taking Raniplex (View Usage) (Dosage: 150mg Per Day) was diagnosed with basedow's disease and. Location: FRANCE , 35 years of age, Patient experienced the following unwanted or unexpected effects: coma acidotic, thrombocytopenia. During the same period patient was treated with LOVENOX (40mg Per Day) (View Lovenox Review and Lovenox Label ), NEO MERCAZOLE TAB (View Neo-mercazole Tab Review and Neo-mercazole Tab Label ), HALDOL (View Haldol Review and Haldol Label ), TERCIAN (View Tercian Review and Tercian Label ), HEPARIN (View Heparin Review and Heparin Label ). Patient was hospitalized.

5035632-3 | Conjunctivitis, Dermatitis Exfoliative, Febrile Bone Marrow Aplasia, Oral Soft Tissue Disorder, Prurigo, Purpura
on Jun 19, 2006 Female patient from FRANCE , 78 years of age, weighting 127.9 lb, was treated with Raniplex (View Usage). Patient had the following side effects: conjunctivitis, dermatitis exfoliative, febrile bone marrow aplasia, oral soft tissue disorder, prurigo, purpura. Raniplex dosage: 1unit Cyclic. During the same period patient was treated with TAXOL (260mg Per Day) (View Taxol Review and Taxol Label ), CIFLOX (800mg Per Day) (View Ciflox Review and Ciflox Label ), CARBOPLATIN (400mg Per Day) (View Carboplatin Review and Carboplatin Label ), ROCEPHIN (2mg Per Day) (View Rocephin Review and Rocephin Label ), ZOPHREN (1amp Per Day) (View Zophren Review and Zophren Label ), SOLU MEDROL (120mg Per Day) (View Solu-medrol Review and Solu-medrol Label ), POLARAMINE (1amp Per Day) (View Polaramine Review and Polaramine Label ), PRIMPERAN TAB (1amp Per Day) (View Primperan Tab Review and Primperan Tab Label ). Patient was hospitalized.

4876535-4 | Rash Maculo-papular, Skin Test Positive
on Jan 03, 2006 Male patient from FRANCE , 39 years of age, was treated with Raniplex (View Usage). After Raniplex was administered, patient had the following side effects: rash maculo-papular, skin test positive. Raniplex dosage: . During the same period patient was treated with CELOCURINE (View Celocurine Review and Celocurine Label ), DIPRIVAN (View Diprivan Review and Diprivan Label ), NIMBEX (View Nimbex Review and Nimbex Label ), SUFENTA (View Sufenta Review and Sufenta Label ), MORPHINE (View Morphine Review and Morphine Label ). Patient was hospitalized.

4817036-9 | Dyspnoea, Electrocardiogram Qt Prolonged, Loss Of Consciousness, Malaise, Torsade De Pointes
Patient was taking Raniplex (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, electrocardiogram qt prolonged, loss of consciousness, malaise, torsade de pointes on Oct 24, 2005 from FRANCE Additional patient health information: Female patient , 46 years of age, was diagnosed with tachycardia, gout (What is gout?), epilepsy (What is epilepsy?) and. Raniplex dosage: 1unit Twice Per Day. During the same period patient was treated with DILTIAZEM HCL (1unit Three Times Per Day) (View Diltiazem Hcl Review and Diltiazem Hcl Label ), COLCHICINE (1unit Per Day) (View Colchicine Review and Colchicine Label ), NEURONTIN (2unit Twice Per Day) (View Neurontin Review and Neurontin Label ), CORTANCYL (20mg Per Day) (View Cortancyl Review and Cortancyl Label ), KLIPAL (2unit Three Times Per Day) (View Klipal Review and Klipal Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), SPECIAFOLDINE (View Speciafoldine Review and Speciafoldine Label ), REMICADE (View Remicade Review and Remicade Label ). Patient was hospitalized.

4771931-8 | Convulsion, Hypotension, Loss Of Consciousness, Shock
Adverse event was reported on Sep 13, 2005 by a Male patient taking Raniplex (View Usage) (Dosage: 1inj Single Dose) . Location: FRANCE , 67 years of age, weighting 145.5 lb, Patient had the following side effects: convulsion, hypotension, loss of consciousness, shock. During the same period patient was treated with CETUXIMAB (650mg Per Day) (View Cetuximab Review and Cetuximab Label ), POLARAMINE (1inj Per Day) (View Polaramine Review and Polaramine Label ), SOLU MEDROL (2inj Per Day) (View Solu-medrol Review and Solu-medrol Label ), DIAMICRON (View Diamicron Review and Diamicron Label ), CORVASAL (View Corvasal Review and Corvasal Label ), CREON (View Creon Review and Creon Label ), HALDOL (View Haldol Review and Haldol Label ), SKENAN (View Skenan Review and Skenan Label ). Patient was hospitalized.

4761493-3 | Anaphylactic Shock, Blood Pressure Decreased, Cardio-respiratory Arrest, Heart Rate Decreased, Loss Of Consciousness, Malaise, Oxygen Saturation Decreased, Vomiting
on Jun 09, 2005 Female patient from FRANCE , 80 years of age, weighting 108.0 lb, was diagnosed with prophylaxis, breast cancer in situ, hypersensitivity and was treated with Raniplex (View Usage). After Raniplex was administered, patient had the following side effects: anaphylactic shock, blood pressure decreased, cardio-respiratory arrest, heart rate decreased, loss of consciousness, malaise, oxygen saturation decreased, vomiting. Raniplex dosage: 300mg Per Day. During the same period patient was treated with ONDANSETRON (8mg Per Day) (View Ondansetron Review and Ondansetron Label ), SOLU MEDROL (80mg Per Day) (View Solu-medrol Review and Solu-medrol Label ), TAXOL (View Taxol Review and Taxol Label ), POLARAMINE (View Polaramine Review and Polaramine Label ). Patient was hospitalized.

4754614-X | Pancytopenia, Thrombocytopenia
on Nov 12, 2004 Male patient from FRANCE , 77 years of age, was diagnosed with abdominal pain upper, choroid melanoma and was treated with Raniplex (View Usage). Patient experienced the following unwanted or unexpected effects: pancytopenia, thrombocytopenia. Raniplex dosage: 150mg Per Day. During the same period patient was treated with DETICENE (1unit Per Day) (View Deticene Review and Deticene Label ), FOTEMUSTINE (1unit Weekly) (View Fotemustine Review and Fotemustine Label ), ONDANSETRON (View Ondansetron Review and Ondansetron Label ), VOGALENE (View Vogalene Review and Vogalene Label ), MEDIATENSYL (View Mediatensyl Review and Mediatensyl Label ), OXAZEPAM (View Oxazepam Review and Oxazepam Label ), XANAX (View Xanax Review and Xanax Label ), ATARAX (View Atarax Review and Atarax Label ). Patient was hospitalized.

4745940-9 | Agitation, Bradycardia, Cardiac Arrest, Cardio-respiratory Arrest, Epilepsy, Sinoatrial Block, Syncope
Patient was taking Raniplex (View Usage). Patient had the following side effects: agitation, bradycardia, cardiac arrest (What is cardiac arrest?), cardio-respiratory arrest, epilepsy (What is epilepsy?), sinoatrial block, syncope on Jul 26, 2005 from FRANCE Additional patient health information: Male patient , 63 years of age, weighting 147.7 lb, . Raniplex dosage: 150mg Per Day. During the same period patient was treated with OMEPRAZOLE (1unit Per Day) (View Omeprazole Review and Omeprazole Label ).

4734771-1 | Agitation, Bradycardia, Cardiac Arrest, Cardio-respiratory Arrest, Epilepsy, Sinoatrial Block, Sinus Bradycardia, Syncope
Adverse event was reported on Jul 26, 2005 by a Male patient taking Raniplex (View Usage) (Dosage: ) was diagnosed with oesophagitis ulcerative and. Location: FRANCE , 63 years of age, weighting 147.7 lb, After Raniplex was administered, patient had the following side effects: agitation, bradycardia, cardiac arrest (What is cardiac arrest?), cardio-respiratory arrest, epilepsy (What is epilepsy?), sinoatrial block, sinus bradycardia, syncope. During the same period patient was treated with OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).

4712245-1 | Pancytopenia, Thrombocytopenia
on Nov 12, 2004 Male patient from FRANCE , 77 years of age, was diagnosed with choroid melanoma and was treated with Raniplex (View Usage). Patient experienced the following unwanted or unexpected effects: pancytopenia, thrombocytopenia. Raniplex dosage: 150mg Per Day. During the same period patient was treated with DETICENE (1unit Per Day) (View Deticene Review and Deticene Label ), FOTEMUSTINE (1unit Weekly) (View Fotemustine Review and Fotemustine Label ), ONDANSETRON (View Ondansetron Review and Ondansetron Label ), VOGALENE (View Vogalene Review and Vogalene Label ), MEDIATENSYL (View Mediatensyl Review and Mediatensyl Label ), OXAZEPAM (View Oxazepam Review and Oxazepam Label ), XANAX (View Xanax Review and Xanax Label ), ATARAX (View Atarax Review and Atarax Label ). Patient was hospitalized.

4706465-X | Pancytopenia, Thrombocytopenia
on Nov 12, 2004 Male patient from FRANCE , 77 years of age, was diagnosed with abdominal pain upper, choroid melanoma and was treated with Raniplex (View Usage). Patient had the following side effects: pancytopenia, thrombocytopenia. Raniplex dosage: 150mg Per Day. During the same period patient was treated with DETICENE (1unit Per Day) (View Deticene Review and Deticene Label ), FOTEMUSTINE (1unit Weekly) (View Fotemustine Review and Fotemustine Label ), ONDANSETRON (View Ondansetron Review and Ondansetron Label ), VOGALENE (View Vogalene Review and Vogalene Label ), MEDIATENSYL (View Mediatensyl Review and Mediatensyl Label ), OXAZEPAM (View Oxazepam Review and Oxazepam Label ), XANAX (View Xanax Review and Xanax Label ), ATARAX (View Atarax Review and Atarax Label ). Patient was hospitalized.

4704403-7 | Anaphylactic Shock, Blood Pressure Decreased, Cardio-respiratory Arrest, Heart Rate Decreased, Loss Of Consciousness, Malaise, Oxygen Saturation Decreased, Vomiting
Patient was taking Raniplex (View Usage). After Raniplex was administered, patient had the following side effects: anaphylactic shock, blood pressure decreased, cardio-respiratory arrest, heart rate decreased, loss of consciousness, malaise, oxygen saturation decreased, vomiting on Jun 09, 2005 from Additional patient health information: Female patient , 81 years of age, weighting 108.0 lb, was diagnosed with prophylaxis and. Raniplex dosage: 300mg Per Day. During the same period patient was treated with ONDANSETRON (8mg Per Day) (View Ondansetron Review and Ondansetron Label ), SOLU MEDROL (80mg Per Day) (View Solu-medrol Review and Solu-medrol Label ). Patient was hospitalized.

4698160-0 | Pancytopenia, Thrombocytopenia
Adverse event was reported on Nov 12, 2004 by a Male patient taking Raniplex (View Usage) (Dosage: 150mg Per Day) was diagnosed with choroid melanoma and. Location: , 77 years of age, Patient experienced the following unwanted or unexpected effects: pancytopenia, thrombocytopenia. During the same period patient was treated with DETICENE (1unit Per Day) (View Deticene Review and Deticene Label ), FOTEMUSTINE (1unit Weekly) (View Fotemustine Review and Fotemustine Label ), ONDANSETRON (View Ondansetron Review and Ondansetron Label ), VOGALENE (View Vogalene Review and Vogalene Label ), MEDIATENSYL (View Mediatensyl Review and Mediatensyl Label ), OXAZEPAM (View Oxazepam Review and Oxazepam Label ), XANAX (View Xanax Review and Xanax Label ), ATARAX (View Atarax Review and Atarax Label ). Patient was hospitalized.

4694677-3 | Blood Pressure Decreased, Cardio-respiratory Arrest, Heart Rate Decreased, Hypersensitivity, Loss Of Consciousness, Malaise, Oxygen Saturation Decreased, Vomiting
on Jun 09, 2005 Female patient from , 81 years of age, weighting 108.0 lb, was treated with Raniplex (View Usage). Patient had the following side effects: blood pressure decreased, cardio-respiratory arrest, heart rate decreased, hypersensitivity, loss of consciousness, malaise, oxygen saturation decreased, vomiting. Raniplex dosage: 300mg Per Day. During the same period patient was treated with ONDANSETRON (8mg Per Day) (View Ondansetron Review and Ondansetron Label ), SOLU MEDROL (8mg Per Day) (View Solu-medrol Review and Solu-medrol Label ). Patient was hospitalized.

4636541-1 | Anaphylactic Shock, Circulatory Collapse, Headache, Hot Flush, Loss Of Consciousness, Malaise
on Apr 06, 2005 Female patient from , 73 years of age, was treated with Raniplex (View Usage). After Raniplex was administered, patient had the following side effects: anaphylactic shock, circulatory collapse, headache (What is headache?), hot flush, loss of consciousness, malaise. Raniplex dosage: 1amp Per Day. During the same period patient was treated with POLARAMINE (1amp Per Day) (View Polaramine Review and Polaramine Label ), SOLU MEDROL (20mgml Single Dose) (View Solu-medrol Review and Solu-medrol Label ).

4592052-3 | Caesarean Section, Epidermolysis Bullosa, Foetal Distress Syndrome, Neonatal Respiratory Distress Syndrome, Small For Dates Baby
Patient was taking Raniplex (View Usage). Patient experienced the following unwanted or unexpected effects: caesarean section, epidermolysis bullosa, foetal distress syndrome, neonatal respiratory distress syndrome, small for dates baby on Feb 17, 2005 from Additional patient health information: Female patient , weighting 4.41 lb, was diagnosed with gastrooesophageal reflux disease and. Raniplex dosage: 3tab Per Day. Patient was hospitalized.

4547458-5 | Aplastic Anaemia, Haemoglobin Decreased, Haemolytic Anaemia, Hyperbilirubinaemia, Jaundice Neonatal
Adverse event was reported on Dec 08, 2004 by a Male patient taking Raniplex (View Usage) (Dosage: 12mck Per Day) was diagnosed with gastrooesophageal reflux disease, haemoglobin decreased and. Location: , weighting 7.72 lb, Patient had the following side effects: aplastic anaemia, haemoglobin decreased, haemolytic anaemia, hyperbilirubinaemia, jaundice neonatal. During the same period patient was treated with PRIMPERAN INJ (18drop Per Day) (View Primperan Inj Review and Primperan Inj Label ), FERROSTRANE (1sp Per Day) (View Ferrostrane Review and Ferrostrane Label ), UVESTEROL (View Uvesterol Review and Uvesterol Label ). Patient was hospitalized.

4497859-9 | Dyspnoea, Interstitial Lung Disease, Pyrexia
on Nov 04, 2004 Female patient from , 84 years of age, was diagnosed with ill-defined disorder and was treated with Raniplex (View Usage). After Raniplex was administered, patient had the following side effects: dyspnoea, interstitial lung disease, pyrexia. Raniplex dosage: . During the same period patient was treated with CORDARONE (200mg Per Day) (View Cordarone Review and Cordarone Label ), VEINAMITOL (View Veinamitol Review and Veinamitol Label ), VASTAREL (View Vastarel Review and Vastarel Label ), HYDREA (View Hydrea Review and Hydrea Label ), ZOCOR (View Zocor Review and Zocor Label ), ACUITEL (View Acuitel Review and Acuitel Label ), PLAVIX (1unit Per Day) (View Plavix Review and Plavix Label ). Patient was hospitalized.