Please choose an event type to view the corresponding MedsFacts report:

DYSPNOEA ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
DYSPNOEA AT REST ( 5 FDA reports)
PAIN ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
PYREXIA ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
PNEUMOCOCCAL INFECTION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MENINGOCOCCAL SEPSIS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
FOETAL MALPOSITION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
DEATH ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONGENITAL FOOT MALFORMATION ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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