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

PNEUMONIA ( 5 FDA reports)
AGEUSIA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
COUGH ( 3 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 3 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BONE SARCOMA ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
EXPOSED BONE IN JAW ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GOITRE ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
SCAPULA FRACTURE ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
INJECTION SITE SCAR ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
MASS ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NODULE ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
NEURALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)

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