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MULTI-ORGAN DISORDER side effect

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Novoseven Side Effects Report #5612200-3
Physician from JAPAN reported NOVOSEVEN problem on Jan 25, 2008. Female patient was diagnosed with off label use, sepsis and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: multi-organ disorder, . NOVOSEVEN dosage: unknown. During the same period patient was treated with VANCOMYCIN HYDROCHLORIDE. Patient died on 01/04/2004.

Hydroxychloroqui Side Effects Report #5573379-5
HYDROXYCHLOROQUINE SULPHATE problem was reported by a Pharmacist from UNITED STATES on Dec 20, 2007. Female patient, weighting 156.0 lb, was diagnosed with polymyalgia rheumatica and was treated with HYDROXYCHLOROQUINE SULPHATE. After drug was administered, patient experienced the following problems/side effects: multi-organ disorder, no therapeutic response, rash, . HYDROXYCHLOROQUINE SULPHATE dosage: 200MG BID PO. Patient was hospitalized. Patient recovered.

Celebrex Side Effects Report #5779462-3
Consumer or non-health professional from UNITED STATES reported CELEBREX problem on June 09, 2008. Female patient, weighting 154.1 lb, was diagnosed with osteoarthritis and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: multi-organ disorder, . CELEBREX dosage: unknown. Patient recovered.

Thymoglobulin Side Effects Report #5355250-7
THYMOGLOBULIN problem was reported by a Physician from TAIWAN, PROVINCE OF CHINA on May 21, 2007. Male patient, weighting 13.23 lb, was diagnosed with stem cell transplant, acute myeloid leukaemia and was treated with THYMOGLOBULIN. After drug was administered, patient experienced the following problems/side effects: multi-organ disorder, pulmonary oedema, shock, . THYMOGLOBULIN dosage: 2.5 MG/KG QD IV. During the same period patient was treated with BUSULFAN. Patient recovered.


Humira Side Effects Report #5654370-7
Health Professional from UNITED KINGDOM reported HUMIRA problem on Feb 26, 2008. Female patient, weighting 147.7 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bronchopneumonia, multi-organ disorder, multi-organ failure, rheumatoid arthritis, sepsis, tuberculosis, . HUMIRA dosage: unknown. During the same period patient was treated with DICLOFENAC, ACETAMINOPHEN. Patient died on 03/15/2007.

Avalide Side Effects Report #5660177-7
AVALIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 10, 2008. Male patient, 50 years of age, weighting 220.0 lb, was diagnosed with hypertension and was treated with AVALIDE. After drug was administered, patient experienced the following problems/side effects: cardiac failure congestive, multi-organ disorder, muscle spasms, oedema peripheral, pneumonia, renal pain, respiratory failure, vomiting, . AVALIDE dosage: unknown. During the same period patient was treated with LISINOPRIL. Patient was hospitalized. Patient recovered.

Kaletra Side Effects Report #5689418-7
Consumer or non-health professional from ROMANIA reported KALETRA problem on Mar 26, 2008. Male patient, weighting 165.3 lb, was diagnosed with hiv infection, acquired immunodeficiency syndrome and was treated with KALETRA. After drug was administered, patient experienced the following problems/side effects: disseminated intravascular coagulation, multi-organ disorder, myocarditis, overdose, pulmonary oedema, systemic inflammatory response syndrome, . KALETRA dosage: unknown. Patient was hospitalized and became disabled. Patient died on 01/09/2008.

Focalin Side Effects Report #5631810-0
FOCALIN problem was reported by a Health Professional from on Feb 15, 2008. Male patient, child 9 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with FOCALIN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal disorder, multi-organ disorder, mycoplasma infection, stevens-johnson syndrome, . FOCALIN dosage: 20 MG, QD. Patient was hospitalized. Patient recovered.

Ibuprofen Side Effects Report #5635912-4
Health Professional from UNITED KINGDOM reported IBUPROFEN problem on Nov 20, 2007. Female patient, 36 years of age, was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: multi-organ disorder, . IBUPROFEN dosage: unknown. Patient was hospitalized. Patient recovered.


Reopro Side Effects Report #5585182-0
REOPRO problem was reported by a Physician from INDIA on Jan 02, 2008. Male patient, 65 years of age, was treated with REOPRO. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, multi-organ disorder, multi-organ failure, pulmonary haemorrhage, . REOPRO dosage: unknown. Patient was hospitalized. Patient died on 01/02/2008.

Humira Side Effects Report #5398055-3
Health Professional from UNITED KINGDOM reported HUMIRA problem on July 16, 2007. Female patient, weighting 147.7 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bronchopneumonia, multi-organ disorder, multi-organ failure, rheumatoid arthritis, sepsis, . HUMIRA dosage: unknown. During the same period patient was treated with DICLOFENAC, ACETAMINOPHEN. Patient died on 03/15/2007.

Humira Side Effects Report #5398055-3
HUMIRA problem was reported by a Health Professional from UNITED KINGDOM on July 16, 2007. Female patient, weighting 147.7 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bronchopneumonia, multi-organ disorder, multi-organ failure, rheumatoid arthritis, sepsis, . HUMIRA dosage: unknown. During the same period patient was treated with DICLOFENAC, ACETAMINOPHEN. Patient died on 03/15/2007.

Digitek Side Effects Report #5764063-3
Consumer or non-health professional from UNITED STATES reported DIGITEK problem on June 06, 2008. Female patient, weighting 120.0 lb, was diagnosed with cardiac disorder and was treated with DIGITEK. After drug was administered, patient experienced the following problems/side effects: eye disorder, multi-organ disorder, . DIGITEK dosage: unknown. Patient recovered.

Boniva Side Effects Report #5699188-4
BONIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 07, 2008. Female patient, 53 years of age, weighting 220.0 lb, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: bone disorder, multi-organ disorder, muscle disorder, suicidal ideation, . BONIVA dosage: unknown. Patient recovered.


Heparin Side Effects Report #5707877-8
Pharmacist from UNITED STATES reported HEPARIN LOCK problem on Apr 17, 2008. Male patient, 66 years of age, weighting 244.9 lb, was diagnosed with central venous catheterisation and was treated with HEPARIN LOCK. After drug was administered, patient experienced the following problems/side effects: hepatic failure, multi-organ disorder, neutrophil count decreased, renal failure acute, rhabdomyolysis, weaning failure, white blood cell count decreased, . HEPARIN LOCK dosage: unknown. During the same period patient was treated with ZOSYN, CHLORIDE. Patient was hospitalized. Patient died on 04/14/2008.

Cerezyme Side Effects Report #5538439-3
CEREZYME problem was reported by a Physician from INDIA on Nov 22, 2007. Male patient, weighting 31.97 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: bacterial infection, blood culture positive, multi-organ disorder, pneumonia, respiratory distress, septic shock, . CEREZYME dosage: unknown. Patient was hospitalized. Patient died on 10/04/2007.

Primaxin Side Effects Report #5564865-2
Pharmacist from UNITED STATES reported PRIMAXIN problem on Dec 13, 2007. Male patient, weighting 174.2 lb, was diagnosed with pneumonia, sepsis and was treated with PRIMAXIN. After drug was administered, patient experienced the following problems/side effects: c-reactive protein increased, multi-organ disorder, renal impairment, shift to the left, toxic epidermal necrolysis, . PRIMAXIN dosage: 250 MG EVERY 6 HRS IV 4 DOSES. Patient was hospitalized. Patient recovered.

Amevive Side Effects Report #5509476-X
AMEVIVE problem was reported by a Physician from UNITED STATES on Oct 24, 2007. Female patient, 57 years of age, weighting 145.1 lb, was diagnosed with psoriasis and was treated with AMEVIVE. After drug was administered, patient experienced the following problems/side effects: ascites, liposarcoma, multi-organ disorder, . AMEVIVE dosage: 15 MG, WEEKLY, INTRAMUSCULAR. Patient was hospitalized. Patient died on 09/28/2007.

Rebif Side Effects Report #5522928-1
Consumer or non-health professional from UNITED STATES reported REBIF problem on Nov 08, 2007. Female patient, 27 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: abdominal mass, abdominal pain upper, multi-organ disorder, . REBIF dosage: unknown. During the same period patient was treated with PREVACID, CYCLOBENZAPRINE, MIRAPEX, TRAZODONE, TOPAMAX, IMITREX, KLONOPIN, SENOKOT. Patient was hospitalized. Patient recovered.


Revlimid Side Effects Report #5779003-0
REVLIMID problem was reported by a Physician from UNITED STATES on June 10, 2008. Male patient, 73 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: febrile neutropenia, infection, multi-organ disorder, . REVLIMID dosage: 25 MG, QD X21 DAYS/28 DAYS, ORAL. Patient died on 05/18/2008.

Heparin Side Effects Report #5705456-X
Pharmacist from UNITED STATES reported HEPARIN problem on Apr 15, 2008. Female patient, 64 years of age, weighting 198.4 lb, was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: anaphylactic reaction, cardiac disorder, multi-organ disorder, shock, . HEPARIN dosage: unknown. Patient died on 04/03/2008.