Recombinant Side Effects
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Recently reported Recombinant Side Effects
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Recombinant Side Effects reported on Patientsville.com
None reported at this time.Recombinant Side Effects reported to FDA
Recombinant Side Effects Report #5350373-0
Physician from UNITED STATES reported Recombinant side effect on June 06, 2007. Male patient, weighting 198.4 lb, was diagnosed with haemorrhage and was treated with Recombinant. After drug was administered, patient experienced the following side effects: atrial thrombosis, cardiac arrest
, pulmonary embolism . Recombinant dosage: unknown. Patient recovered.
Recombinant Side Effects Report #5069865-7
Recombinant side effect was reported by a Physician from FRANCE on July 10, 2006. Male patient, 13 years of age, was diagnosed with factor viii deficiency and was treated with Recombinant. After drug was administered, patient experienced the following side effects: activated partial thromboplastin time prolonged, haemarthrosis. Recombinant dosage: unknown. During the same period patient was treated with HEXATRIONE. Patient was hospitalized. Patient recovered.
Recombinant Side Effects Report #5097918-6
Pharmacist from UNITED STATES reported Recombinant side effect on Sept 05, 2006. Female patient, weighting 251.3 lb, was diagnosed with international normalised ratio increased and was treated with Recombinant. After drug was administered, patient experienced the following side effects: basilar artery thrombosis, cerebral infarction. Recombinant dosage: 4.8 MG 3 DOSES IV BOLUS. Patient was hospitalized. Patient recovered.
Recombinant Side Effects Report #5766565-2
Recombinant side effect was reported by a Pharmacist from UNITED STATES on June 11, 2008. Female patient, 73 years of age, weighting 156.5 lb, was diagnosed with gastrointestinal haemorrhage, wound secretion and was treated with Recombinant. After drug was administered, patient experienced the following side effects: aphasia
, depressed level of consciousness, dysarthria, mental status changes, speech disorder. Recombinant dosage: unknown. During the same period patient was treated with RECOMBINANT FACTOR. Patient was hospitalized. Patient recovered.Recombinant Side Effects Report #5966551-3
Health Professional from CANADA reported Recombinant side effect on Nov 18, 2008. Female patient, 20 years of age, was diagnosed with thrombocytopenia and was treated with Recombinant. After drug was administered, patient experienced the following side effects: analgesia, blood creatine increased, blood urea increased, depressed level of consciousness, oedema peripheral, pulmonary oedema, respiratory depression, somnolence. Recombinant dosage: unknown. During the same period patient was treated with DAPSONE, AMITRIPTYLINE, NEUPOGEN, MORPHINE, PHENOBARBITAL. Patient recovered.
Recombinant Side Effects Report #6130311-3
Recombinant side effect was reported by a Health Professional from CANADA on Mar 17, 2009. Female patient, 20 years of age, weighting 79.37 lb, was diagnosed with thrombocytopenia, prophylaxis, pain
, sedation and was treated with Recombinant. After drug was administered, patient experienced the following side effects: analgesia, blood creatinine increased, blood urea increased, depressed level of consciousness, oedema peripheral, pulmonary oedema, respiratory depression, somnolence. Recombinant dosage: unknown. During the same period patient was treated with DAPSONE, AMITRIPTYLINE, MORPHINE, PHENOBARBITAL. Patient was hospitalized. Patient recovered.Recombinant Side Effects Report #4644692-0
Consumer or non-health professional from reported Recombinant side effect on Apr 13, 2005. Female patient, 33 years of age, was diagnosed with in vitro fertilisation and was treated with Recombinant. After drug was administered, patient experienced the following side effects: myocardial infarction, ovarian hyperstimulation syndrome. Recombinant dosage: unknown. Patient was hospitalized. Patient died.
Recombinant Side Effects Report #4675045-7
Recombinant side effect was reported by a Physician from on May 10, 2005. Female patient was diagnosed with in vitro fertilisation, luteal phase deficiency and was treated with Recombinant. After drug was administered, patient experienced the following side effects: amniocentesis abnormal, caesarean section, congenital anomaly, inguinal hernia. Recombinant dosage: unknown. During the same period patient was treated with MENOPAUSAL GONADOTROPIN, CETRORELIX, CHORIONIC GONADOTROPIN, OSTRADIOL, PROGESTERONE IN OIL. Patient was hospitalized. Patient recovered.
Recombinant Side Effects Report #4675091-3
Physician from reported Recombinant side effect on May 10, 2005. Female patient was diagnosed with in vitro fertilisation, luteal phase deficiency and was treated with Recombinant. After drug was administered, patient experienced the following side effects: apgar score low, blood gonadotrophin increased, blood pressure increased, caesarean section, congenital genital malformation female, foetal movements decreased, genitalia external ambiguous, gonadal dysgenesis, hermaphroditism. Recombinant dosage: unknown. During the same period patient was treated with MENOTROPINS, CETRORELIX, CHORIONIC GONADOTROPIN, ESTRADIOL, PROGESTERONE IN OIL. Patient was hospitalized. Patient recovered.