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

HAEMORRHAGIC DISORDER ( 6 FDA reports)
BRONCHITIS CHRONIC ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
HEPATIC ENZYME ABNORMAL ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
FALL ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
DELIRIUM ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LACERATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
STRESS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)

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