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

PNEUMONIA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HEPATIC ENZYME DECREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALL ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
THYROID ATROPHY ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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