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

VENA CAVA THROMBOSIS ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
OVARIAN CYST ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
FALL ( 4 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
CRYING ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
RESTLESSNESS ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
AGITATION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
INCONTINENCE ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MELAENA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
CHOREA ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)

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