Have You experienced a side effect?
and Vote

Yes, Severe
Yes, Moderate
Yes, Minor
No
Discuss Results
1.5 million people annually are harmed from drug errors. Side Effects Reported Today:

Don't Risk Your Health!
Ask a Health Expert Now


HAEMODYNAMIC INSTABILITY side effect

What is HAEMODYNAMIC INSTABILITY ?
Help Community - Describe Your Side Effect   Search FDA Side Effects   Ask Health Expert   HAEMODYNAMIC INSTABILITY and Recently Reported Side Effects   HAEMODYNAMIC INSTABILITY and 15 most Active Side Effect polls   HAEMODYNAMIC INSTABILITY and featured health surveys   Substances toxic to Health   Recent Hospital reviews   Comments about Side Effects   Hospital Quality reviews   Homecare Quality reviews
Health Expert

A Health Expert wants to answer your question.

Please provide details below.



Drugs associated with HAEMODYNAMIC INSTABILITY

ALTACE  AMBISOME  AMEVIVE  AMIODARONE  ANGIOMAX  ARAVA  AUGMENTIN  AZATHIOPRINE  CIPROFLOXACIN  CLOZAPINE  COLCHICINE  COVERSYL  CUBICIN  CYCLOSPORINE  DANTOLENE  DASATINIB  DIGOXIN  EPTIFIBATIDE  ETOMIDATE  FAMOTIDINE  FORTUM  HEPARIN  HUMIRA  HYDROXYCHLOROQUI IBUPROFEN  LANOXIN  LIORESAL  LISINOPRIL  MIRANOVA  MIRTAZAPINE  MITOXANTRONE  MYCOPHENOLATE  NEUPOGEN  NIASTASE  NITRIC  NOVOSEVEN  OXALIPLATIN  PITOCIN  PREDNISONE  PROFLOX  PROGRAF  PROPOFOL  PROSTIN  PROTAMINE  RAMIPRIL  RANITIDINE  RITUXIMAB  SCOPOLAMINE  SIMVASTATIN  SUPRANE  THYMOGLOBULIN  TRACLEER  VELCADE  VINCRISTINE  ZANTAC  ZOCOR  


Hydroxychloroqui Side Effects Report #5655588-X
Physician from NETHERLANDS reported HYDROXYCHLOROQUINE SULPHATE problem on Mar 03, 2008. Female patient, 37 years of age, was treated with HYDROXYCHLOROQUINE SULPHATE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, overdose, . HYDROXYCHLOROQUINE SULPHATE dosage: unknown. Patient was hospitalized. Patient recovered.

Prostin Side Effects Report #5689519-3
PROSTIN E problem was reported by a Physician from SWITZERLAND on Mar 19, 2008. Male patient, 16 years of age, was diagnosed with liver transplant and was treated with PROSTIN E. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, pyrexia, systemic inflammatory response syndrome, . PROSTIN E dosage: unknown. During the same period patient was treated with SIMULECT, VANCOMYCIN, ROCEPHIN, METRONIDAZOLE, MERONEM, DIFLUCAN, CYMEVENE. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5689697-6
Physician from UNITED STATES reported PROGRAF problem on Mar 18, 2008. Female patient, 29 years of age, was diagnosed with heart transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, heart transplant rejection, . PROGRAF dosage: unknown. Patient died on 02/01/2008.

Prednisone Side Effects Report #5624582-7
PREDNISONE problem was reported by a Pharmacist from UNITED STATES on Feb 08, 2008. Female patient, 63 years of age, was diagnosed with crohn's disease, hyperlipidaemia and was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, myopathy, pneumocystis jiroveci pneumonia, . PREDNISONE dosage: ORAL;20.0 MILLIGRAM. During the same period patient was treated with SIMVASTATIN. Patient was hospitalized. Patient recovered.


Protamine Side Effects Report #5534532-X
Pharmacist from UNITED STATES reported PROTAMINE SULPHATE problem on Dec 04, 2007. Male patient, 74 years of age, was diagnosed with coronary artery bypass and was treated with PROTAMINE SULPHATE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, no therapeutic response, post procedural haemorrhage, . PROTAMINE SULPHATE dosage: 450MG ONCE IV. During the same period patient was treated with PROTAMINE SULPHATE, HEPARIN, APROTINEN, STANDARD OPERATIVE PROTOCOL ANESTHETICS, CEPHALOSPORIN, CARDIPLEGIA SOLUTIONS. Patient recovered.

Novoseven Side Effects Report #5504953-X
NOVOSEVEN problem was reported by a Physician from ISRAEL on Oct 29, 2007. Female patient was diagnosed with haemorrhage and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, . NOVOSEVEN dosage: 7.2 MG, UNK. Patient died.

Velcade Side Effects Report #5534952-3
Physician from CHINA reported VELCADE problem on Nov 21, 2007. Male patient, 61 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, leukocytoclastic vasculitis, malnutrition, multi-organ failure, refusal of treatment by patient, toxic epidermal necrolysis, . VELCADE dosage: 1.30 MG/M2, IV BOLUS. Patient was hospitalized. Patient died on 11/26/2006.

Velcade Side Effects Report #5488965-0
VELCADE problem was reported by a Physician from CHINA on Oct 04, 2007. Male patient, 61 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, leukocytoclastic vasculitis, malnutrition, multi-organ failure, pain, refusal of treatment by patient, toxic epidermal necrolysis, . VELCADE dosage: 1.30 MG/M2, IV BOLUS. Patient was hospitalized. Patient died.

Novoseven Side Effects Report #5490352-6
Physician from ITALY reported NOVOSEVEN problem on Oct 08, 2007. Male patient, weighting 183.0 lb, was diagnosed with traumatic haemorrhage, sedation, prophylaxis and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, postoperative wound infection, . NOVOSEVEN dosage: unknown. During the same period patient was treated with PROPOFOL, FENTANYL, NORCURON, KETAMINA, CEFAZOLINA, IPNOVEL. Patient was hospitalized. Patient recovered.


Velcade Side Effects Report #5500122-8
VELCADE problem was reported by a Physician from CHINA on Oct 18, 2007. Male patient, 61 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, leukocytoclastic vasculitis, malnutrition, multi-organ failure, refusal of treatment by patient, toxic epidermal necrolysis, . VELCADE dosage: 1.30 MG/M2, IV BOLUS. Patient was hospitalized. Patient died on 11/26/2006.

Angiomax Side Effects Report #5500189-7
Physician from CANADA reported ANGIOMAX problem on Oct 01, 2007. Male patient, 83 years of age, weighting 145.5 lb, was diagnosed with coronary artery bypass, heparin-induced thrombocytopenia and was treated with ANGIOMAX. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, haemothorax, procedural complication, . ANGIOMAX dosage: 50 MG, INTRAVENOUS. Patient died on 02/21/2007.

Coversyl Side Effects Report #5445956-3
COVERSYL problem was reported by a Health Professional from FRANCE on Aug 28, 2007. Male patient, 79 years of age, was diagnosed with ill-defined disorder and was treated with COVERSYL. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, hyperkalaemia, lung disorder, multi-organ failure, orthopnoea, pleural effusion, pneumonitis, renal failure acute, . COVERSYL dosage: DAILY DOSE: 2 MILLIGRAM(S). During the same period patient was treated with AMIODARONE, DIGOXIN, PLAVIX. Patient was hospitalized. Patient died on 07/15/2007.

Mycophenolate Side Effects Report #5455210-1
Consumer or non-health professional from MEXICO reported MYCOPHENOLATE MOFETIL problem on Sept 14, 2007. Female patient, 54 years of age, was diagnosed with renal transplant and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, hypotension, klebsiella infection, multi-organ failure, postoperative wound infection, renal impairment, renal vessel disorder, respiratory failure, septic shock, . MYCOPHENOLATE MOFETIL dosage: unknown. During the same period patient was treated with PREDNISONE, VALCYTE, CYCLOSPORINE. Patient was hospitalized and became disabled. Patient died on 07/05/2007.

Novoseven Side Effects Report #5458182-9
NOVOSEVEN problem was reported by a Physician from ITALY on Sept 13, 2007. Male patient, weighting 187.4 lb, was diagnosed with traumatic haemorrhage, sedation, analgesia, prophylaxis and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, . NOVOSEVEN dosage: unknown. During the same period patient was treated with PROPOFOL, FENTANYL, NORCURON, KETAMINA, IPNOVEL, CEFAZOLINA. Patient was hospitalized. Patient recovered.


Novoseven Side Effects Report #5469289-4
Physician from ITALY reported NOVOSEVEN problem on Sept 20, 2007. Male patient, weighting 187.4 lb, was diagnosed with traumatic haemorrhage, sedation, analgesia, prophylaxis and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, . NOVOSEVEN dosage: unknown. During the same period patient was treated with PROPOFOL, FENTANYL, NORCURON, KETAMINA, IPNOVEL, CEFAZOLINA. Patient was hospitalized. Patient recovered.

Niastase Side Effects Report #5403704-7
NIASTASE problem was reported by a Physician from CANADA on July 24, 2007. Male patient, 52 years of age, weighting 165.3 lb, was diagnosed with haemorrhage and was treated with NIASTASE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, . NIASTASE dosage: 2.4 MG, BID. During the same period patient was treated with ARGATROBAN. Patient died.

Mycophenolate Side Effects Report #5406923-9
Consumer or non-health professional from MEXICO reported MYCOPHENOLATE MOFETIL problem on Aug 03, 2007. Female patient, 54 years of age, was diagnosed with renal transplant and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, hypotension, klebsiella infection, multi-organ failure, postoperative wound infection, renal impairment, renal vessel disorder, respiratory failure, septic shock, . MYCOPHENOLATE MOFETIL dosage: unknown. During the same period patient was treated with PREDNISONE, VALCYTE, CYCLOSPORINE. Patient was hospitalized and became disabled. Patient died on 07/05/2007.

Eptifibatide Side Effects Report #5427617-X
EPTIFIBATIDE problem was reported by a Physician from FRANCE on Aug 13, 2007. Female patient, 59 years of age, was treated with EPTIFIBATIDE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, haemoglobin decreased, melaena, multi-organ failure, red blood cell count decreased, . EPTIFIBATIDE dosage: unknown. During the same period patient was treated with CLOPIDOGREL BISULPHATE, LYSINE ASPIRIN, HEPARIN. Patient died on 07/18/2007.

Arava Side Effects Report #5429204-6
Pharmacist from UNITED STATES reported ARAVA problem on Aug 27, 2007. Female patient, weighting 130.0 lb, was diagnosed with arthritis and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, pneumonia aspiration, stevens-johnson syndrome, toxic epidermal necrolysis, . ARAVA dosage: unknown. Patient recovered.


Mycophenolate Side Effects Report #5393290-2
MYCOPHENOLATE MOFETIL problem was reported by a Consumer or non-health professional from MEXICO on July 18, 2007. Female patient, 54 years of age, was diagnosed with renal transplant and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, hypotension, klebsiella infection, multi-organ failure, postoperative wound infection, renal impairment, renal vessel disorder, respiratory failure, septic shock, . MYCOPHENOLATE MOFETIL dosage: unknown. During the same period patient was treated with PREDNISONE, VALCYTE, CYCLOSPORINE. Patient was hospitalized and became disabled. Patient died on 07/05/2007.

Niastase Side Effects Report #5395089-X
Physician from CANADA reported NIASTASE problem on July 19, 2007. Male patient was diagnosed with haemorrhage and was treated with NIASTASE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, . NIASTASE dosage: 2.4 MG, BID. During the same period patient was treated with ARGATROBAN. Patient died.

Vincristine Side Effects Report #5403384-0
VINCRISTINE problem was reported by a Health Professional from TURKEY on July 22, 2007. Male patient, 69 years of age, was diagnosed with hodgkin's disease and was treated with VINCRISTINE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, haemoglobin decreased, lower gastrointestinal haemorrhage, platelet count decreased, . VINCRISTINE dosage: unknown. During the same period patient was treated with CYCLOPHOSPHAMIDE, DOXORUBICIN, PREDNISONE. Patient recovered.

Mycophenolate Side Effects Report #5393290-2
Consumer or non-health professional from MEXICO reported MYCOPHENOLATE MOFETIL problem on July 18, 2007. Female patient, 54 years of age, was diagnosed with renal transplant and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, hypotension, klebsiella infection, multi-organ failure, postoperative wound infection, renal impairment, renal vessel disorder, respiratory failure, septic shock, . MYCOPHENOLATE MOFETIL dosage: unknown. During the same period patient was treated with PREDNISONE, VALCYTE, CYCLOSPORINE. Patient was hospitalized and became disabled. Patient died on 07/05/2007.

Niastase Side Effects Report #5395089-X
NIASTASE problem was reported by a Physician from CANADA on July 19, 2007. Male patient was diagnosed with haemorrhage and was treated with NIASTASE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, . NIASTASE dosage: 2.4 MG, BID. During the same period patient was treated with ARGATROBAN. Patient died.

Vincristine Side Effects Report #5403384-0
Health Professional from TURKEY reported VINCRISTINE problem on July 22, 2007. Male patient, 69 years of age, was diagnosed with hodgkin's disease and was treated with VINCRISTINE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, haemoglobin decreased, lower gastrointestinal haemorrhage, platelet count decreased, . VINCRISTINE dosage: unknown. During the same period patient was treated with CYCLOPHOSPHAMIDE, DOXORUBICIN, PREDNISONE. Patient recovered.

Thymoglobulin Side Effects Report #5794372-3
THYMOGLOBULIN problem was reported by a Physician from UNITED STATES on June 03, 2008. Female patient, 19 years of age, was diagnosed with heart transplant and was treated with THYMOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, hypertension, hyperthermia malignant, hypotension, hypoxia, nervous system disorder, renal failure, . THYMOGLOBULIN dosage: 40 MG, INTRAVENOUS. Patient died.

Famotidine Side Effects Report #5370377-1
Pharmacist from UNITED STATES reported FAMOTIDINE problem on June 25, 2007. Male patient, weighting 185.2 lb, was diagnosed with prophylaxis, stress ulcer and was treated with FAMOTIDINE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, platelet count decreased, post procedural complication, . FAMOTIDINE dosage: 20MG IV DAILY. During the same period patient was treated with INTRAAORTIC BALLOON PUMP. Patient was hospitalized. Patient recovered.

Zocor Side Effects Report #5335150-9
ZOCOR problem was reported by a Physician from UNITED KINGDOM on Jan 19, 2007. Male patient, 54 years of age, was treated with ZOCOR. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, hypotension, overdose, . ZOCOR dosage: unknown. During the same period patient was treated with RAMIPRIL, RANITIDINE. Patient was hospitalized. Patient recovered.

Ramipril Side Effects Report #5284564-4
Consumer or non-health professional from UNITED KINGDOM reported RAMIPRIL problem on Mar 26, 2007. Male patient, 54 years of age, was treated with RAMIPRIL. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, overdose, . RAMIPRIL dosage: unknown. During the same period patient was treated with RANITIDINE, SIMVASTATIN. Patient was hospitalized. Patient recovered.

Zantac Side Effects Report #5300005-2
ZANTAC problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 30, 2007. Male patient, 54 years of age, was treated with ZANTAC. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, hypotension, overdose, . ZANTAC dosage: 4500 MG / ORAL. During the same period patient was treated with RAMIPRIL, SIMVASTATIN. Patient was hospitalized. Patient recovered.

Amiodarone Side Effects Report #5305613-0
Physician from JAPAN reported AMIODARONE problem on Apr 04, 2007. Male patient, 76 years of age, was diagnosed with ventricular tachycardia and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, interstitial lung disease, renal failure, respiratory failure, . AMIODARONE dosage: 200 MG/DAY. Patient was hospitalized. Patient died.

Velcade Side Effects Report #5281189-1
VELCADE problem was reported by a Physician from SPAIN on Mar 16, 2007. Male patient, 65 years of age, weighting 143.3 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, hypotension, ileus paralytic, . VELCADE dosage: 2.30 MG, INTRAVENOUS. During the same period patient was treated with MELPHALAN, PREDNISONE. Patient recovered.

Proflox Side Effects Report #5649927-3
Physician from SPAIN reported PROFLOX problem on Feb 21, 2008. Male patient, 70 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with PROFLOX. After drug was administered, patient experienced the following problems/side effects: anaphylactic reaction, haemodynamic instability, oedema peripheral, oxygen saturation decreased, suffocation feeling, tachycardia, . PROFLOX dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 400 MG. Patient was hospitalized. Patient recovered.

Novoseven Side Effects Report #5662719-4
NOVOSEVEN problem was reported by a Physician from ITALY on Mar 06, 2008. Male patient, weighting 183.0 lb, was diagnosed with traumatic haemorrhage, sedation, analgesia, neuromuscular blockade, prophylaxis and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage, haemodynamic instability, postoperative wound infection, . NOVOSEVEN dosage: unknown. During the same period patient was treated with PROPOFOL, FENTANYL, NORCURON, KETAMINA, CEFAZOLINA, IPNOVEL. Patient was hospitalized. Patient recovered.

Ranitidine Side Effects Report #5671380-4
Health Professional from UNITED KINGDOM reported RANITIDINE problem on Mar 27, 2007. Male patient, 54 years of age, was treated with RANITIDINE. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, haemodynamic instability, overdose, . RANITIDINE dosage: 4500 MG;ORAL. During the same period patient was treated with SIMVASTATIN. Patient was hospitalized. Patient recovered.

Angiomax Side Effects Report #5691490-5
ANGIOMAX problem was reported by a Physician from UNITED STATES on Mar 17, 2008. Female patient, 73 years of age, was diagnosed with coronary artery bypass and was treated with ANGIOMAX. After drug was administered, patient experienced the following problems/side effects: cardiac arrest, haemodynamic instability, low cardiac output syndrome, myocardial infarction, post procedural complication, . ANGIOMAX dosage: 0.75 MG/KG, SINGLE, IV BOLUS. Patient died.

Novoseven Side Effects Report #5634476-9
Physician from ITALY reported NOVOSEVEN problem on Feb 14, 2008. Male patient, weighting 183.0 lb, was diagnosed with traumatic haemorrhage, sedation, analgesia, neuromuscular blockade, prophylaxis and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage, haemodynamic instability, postoperative wound infection, . NOVOSEVEN dosage: unknown. During the same period patient was treated with PROPOFOL, FENTANYL, NORCURON, KETAMINA, CEFAZOLINA, IPNOVEL. Patient was hospitalized. Patient recovered.

Tracleer Side Effects Report #5587555-9
TRACLEER problem was reported by a Consumer or non-health professional from NETHERLANDS on Dec 24, 2007. Male patient, 79 years of age, weighting 156.5 lb, was diagnosed with pulmonary hypertension and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: dyspnoea exertional, haemodynamic instability, . TRACLEER dosage: 125 MG, BID, ORAL; 62.5 MG, BID, ORAL. Patient died on 10/17/2007.

Vincristine Side Effects Report #5565910-0
Physician from NETHERLANDS reported VINCRISTINE problem on Nov 28, 2007. Male patient, child 5 years of age, was treated with VINCRISTINE. After drug was administered, patient experienced the following problems/side effects: fungal sepsis, haemodynamic instability, lactic acidosis, pancytopenia, respiratory failure, systemic mycosis, . VINCRISTINE dosage: unknown. During the same period patient was treated with PREDNISONE, DAUNORUBICIN, ASPARAGINE. Patient was hospitalized. Patient died.

Lioresal Side Effects Report #5573945-7
LIORESAL problem was reported by a Physician from UNITED STATES on Dec 10, 2007. Male patient, child 6 years of age, was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: cardiac arrest, haemodynamic instability, hyperglycaemia, hypernatraemia, hypotension, metabolic acidosis, pulmonary oedema, respiratory distress, skin erosion, . LIORESAL dosage: unknown. Patient died on 09/25/2007.

Scopolamine Side Effects Report #5580194-5
Physician from UNITED STATES reported SCOPOLAMINE problem on Dec 27, 2007. Female patient, 68 years of age, weighting 198.0 lb, was diagnosed with motion sickness and was treated with SCOPOLAMINE. After drug was administered, patient experienced the following problems/side effects: blood pressure fluctuation, haemodynamic instability, . SCOPOLAMINE dosage: unknown. During the same period patient was treated with CLONAZEPAM, ATENOLOL, ASPIRIN, VYTORIN, ACTONEL, OMEGA. Patient recovered.

Novoseven Side Effects Report #5518030-5
NOVOSEVEN problem was reported by a Physician from ITALY on Nov 05, 2007. Male patient, weighting 183.0 lb, was diagnosed with traumatic haemorrhage, sedation, analgesia, prophylaxis and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage, haemodynamic instability, postoperative wound infection, . NOVOSEVEN dosage: unknown. During the same period patient was treated with PROPOFOL, FENTANYL, NORCURON, KETAMINA, CEFAZOLINA, IPNOVEL. Patient was hospitalized. Patient recovered.

Angiomax Side Effects Report #5527192-5
Consumer or non-health professional from UNITED STATES reported ANGIOMAX problem on Nov 08, 2007. Male patient, 58 years of age, was diagnosed with cardiac ablation and was treated with ANGIOMAX. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, haemodynamic instability, . ANGIOMAX dosage: unknown. Patient recovered.

Pitocin Side Effects Report #5478411-5
PITOCIN problem was reported by a Physician from UNITED KINGDOM on Sept 24, 2007. Female patient was treated with PITOCIN. After drug was administered, patient experienced the following problems/side effects: acute right ventricular failure, haemodynamic instability, hypotension, pulmonary arterial pressure increased, right atrial pressure increased, . PITOCIN dosage: unknown. During the same period patient was treated with PROSTACYCLIN, HEPARIN, MIDAZOLAM, FENTANYL, THIOPENTAL, SUXAMETHONIUM CHLORIDE. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5500632-3
Physician from UNITED STATES reported PROGRAF problem on Oct 09, 2007. Male patient, 71 years of age, was diagnosed with heart transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: cardiac failure, haemodynamic instability, heart transplant rejection, . PROGRAF dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL, CORTICOSTEROIDS, PREDNISONE. Patient died.

Novoseven Side Effects Report #5502707-1
NOVOSEVEN problem was reported by a Physician from ITALY on Oct 26, 2007. Male patient, weighting 183.0 lb, was diagnosed with traumatic haemorrhage, sedation, prophylaxis and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage, haemodynamic instability, postoperative wound infection, . NOVOSEVEN dosage: unknown. During the same period patient was treated with PROPOFOL, FENTANYL CITRATE, FENTANYL CITRATE, NORCURON, KETAMINA, CEFAZOLINA, IPNOVEL. Patient was hospitalized. Patient recovered.

Propofol Side Effects Report #5455737-2
Physician from UNITED STATES reported PROPOFOL problem on Sept 05, 2007. Female patient, 29 years of age, was diagnosed with induction of anaesthesia, maintenance of anaesthesia and was treated with PROPOFOL. After drug was administered, patient experienced the following problems/side effects: circulatory collapse, haemodynamic instability, hypotension, metabolic acidosis, no therapeutic response, propofol infusion syndrome, rhabdomyolysis, . PROPOFOL dosage: 4 - 12 MG/KG/H, INFUSION. During the same period patient was treated with NEUROMUSCULAR BLOCKER, MANNITOL, EPINEPHRINE. Patient died.

Ambisome Side Effects Report #5472516-0
AMBISOME problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Sept 10, 2007. Male patient, 69 years of age, was diagnosed with systemic candida and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, leukopenia, . AMBISOME dosage: 350 MG, BID, IV NOS. During the same period patient was treated with VANCOMYCIN HYDROCHLORIDE, IMIPENEM, HALOPERIDOL, INSULIN, CARVEDILOL, FUROSEMIDE, VITAMINS, CAPTOPRIL. Patient died on 08/25/2007.

Humira Side Effects Report #5404905-4
Physician from AUSTRIA reported HUMIRA problem on July 30, 2007. Male patient, weighting 189.6 lb, was diagnosed with polychondritis, coronary artery disease, osteoporosis, prophylaxis against gastrointestinal ulcer, type 2 diabetes mellitus, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: haemodynamic instability, multi-organ failure, pneumonia, renal failure acute, sepsis, syncope, . HUMIRA dosage: unknown. During the same period patient was treated with EBETREXAT, ASPIRIN, RISEDRONATE, LEKOVIT CA, ESOMEPRAZOLE MAGNESIUM, GLIMEPIRIDE, METOPROLOL SUCCINATE, LISINOPRIL. Patient was hospitalized. Patient died on 05/28/2007.

Rituximab Side Effects Report #5777922-2
RITUXIMAB problem was reported by a Physician from FRANCE on June 05, 2008. Female patient was diagnosed with diffuse large b-cell lymphoma and was treated with RITUXIMAB. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage, haemodynamic instability, thrombocytopenia, . RITUXIMAB dosage: 375 MG/M2, Q3W. During the same period patient was treated with CISPLATIN, CYTARABINE, DEXAMETHASONE, LENOGRASTIM. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5788951-7
Health Professional from FRANCE reported VELCADE problem on June 16, 2008. Male patient, 62 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: disease progression, haemodynamic instability, lung infection pseudomonal, multi-organ disorder, obstructive airways disorder, pneumonia haemophilus, pulmonary embolism, renal failure, respiratory distress, . VELCADE dosage: 2.3 MG, INTRAVENOUS. During the same period patient was treated with DEXAMEHASONE. Patient died on 04/06/2008.

PatientsVille.com does not provide medical advice, diagnosis or treatment. The information 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. We hope you found our information about HAEMODYNAMIC INSTABILITY side effects helpful. 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. Thank you for visiting Patientsville.net. Hope you enjoyed finding information on medications and found answers to Your Questions about HAEMODYNAMIC INSTABILITY