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

PNEUMONIA ( 7 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
ARTHRITIS SALMONELLA ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
BREATH SOUNDS ABNORMAL ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 4 FDA reports)
LIPOMA ( 4 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
SCIATICA ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
TREMOR ( 4 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
AMNESIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
RASH ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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